Ellis van Creveld syndrome (EVC) - 1353 nt intron 14 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.91096
gtaagaccagcatggtggccccacccattccagacaggcggtgcccctgcagcaggcccc  c.2097+60

         .         .         .         .         .         .  g.91156
agcttccagcaggtttgccagaacccgaatcctatcacccttggtgctgcagggtgcggt  c.2097+120

         .         .         .         .         .         .  g.91216
attcattcgccggggctgccatagcaaggtcccacagaccgggcagcttacactgcacac  c.2097+180

         .         .         .         .         .         .  g.91276
atttccctgctcaccatcctggaggccagaattcggagatcagggtgtgggcagggccgc  c.2097+240

         .         .         .         .         .         .  g.91336
tttgattctgagaccgcactccctggcttgtagatgactgtcttcaacctgtgtcctcca  c.2097+300

         .         .         .         .         .         .  g.91396
ggtccttcctctgtgggtgtcccatctcttataaggacaccaggcatattggatcaaggc  c.2097+360

         .         .         .         .         .         .  g.91456
ccacgttaatgacctcacttgaccttaatcacctcctcaaaggcactatccacttactga  c.2097+420

         .         .         .         .         .         .  g.91516
cctcccattttgaagtacttggggtcagggcttcaacatacaaattttgagaggacacaa  c.2097+480

         .         .         .         .         .         .  g.91576
tttaaccataacaagtggagacagtggagcccccgtaggggccacccatgtaccaaaagt  c.2097+540

         .         .         .         .         .         .  g.91636
ttttagtatcactgatataatgagaaatatatactggaaaaaccatacggaatcagaggg  c.2097+600

         .         .         .         .         .         .  g.91696
ggacaggtgcagttgtcattgggggtatggtagagaaggcctctgtggtctctttgaagt  c.2097+660

         .         g.91713
gtgataacagatcgaaa  c.2097+677

--------------------- middle of intron ---------------------
                                g.91714           .           g.91729
                                c.2098-676  gaaataattagtaagt  c.2098-661

.         .         .         .         .         .           g.91789
tgtagagctgggagttacacccaggtaggctggctccaggcctcctgcatgtagccacca  c.2098-601

.         .         .         .         .         .           g.91849
agctctgggagcagctgctgctctttgacccatgaatgaggcacaagcccacagtctctt  c.2098-541

.         .         .         .         .         .           g.91909
aagctctatccaggagagctccgaggagcaggcaggactcacggacctcgctacagcccc  c.2098-481

.         .         .         .         .         .           g.91969
gctcacttctttctctcttatttctacaaataaaggcagtcctcagagccctgtgtgccc  c.2098-421

.         .         .         .         .         .           g.92029
tgcctcagcttctgtgatatcctgagactcacatctggcttcaaacctggctctgctgtg  c.2098-361

.         .         .         .         .         .           g.92089
tgactttagaaagttacttaacttctctgagccttcgtgtcctcctcagtgctagtgttc  c.2098-301

.         .         .         .         .         .           g.92149
aggtctcatgatgttctagaaggatgagcaaggccccccatcttgtgaggggccatagat  c.2098-241

.         .         .         .         .         .           g.92209
ggtactgggcacgcagttgatgctcaataaatgccctttttctggggacacagacaccta  c.2098-181

.         .         .         .         .         .           g.92269
acagacacctaacctcatccattgatttttgcaagcccagaggccacctctttctgccct  c.2098-121

.         .         .         .         .         .           g.92329
ttctccatcccttttccaacccctgggccctggataggaccagccccacatcccagtcct  c.2098-61

.         .         .         .         .         .           g.92389
ggccagagcttctctgtgagaggagcacttggcccctgctcccagtcctttccctcccag  c.2098-1