Ellis van Creveld syndrome (EVC) - 502 nt intron 20 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.104314
gtatgactgggccccggacctgttgcctgtggctgggtttggtaaatgcactcagctgct  c.2894+60

         .         .         .         .         .         .  g.104374
gtgtgccaaaagtcagggcaggaaaatcatcagtcccctcagaggcattaaatgtgaagg  c.2894+120

         .         .         .         .         .         .  g.104434
ttcaagaaatgacagatatgaacgtaatttgtgggcagtaagccatgatgataccagggg  c.2894+180

         .         .         .         .         .         .  g.104494
tgccacatggctgttacccttcctgtttgtgtctcatttggccagatgagccttgaccta  c.2894+240

         .   g.104505
cctccacaccc  c.2894+251

--------------------- middle of intron ---------------------
                                     g.104506     .           g.104516
                                     c.2895-251  cattggcatcc  c.2895-241

.         .         .         .         .         .           g.104576
agcctgaagtgttgggcagtcccttctttgaccagggatggctgtggtcatggcacttgg  c.2895-181

.         .         .         .         .         .           g.104636
atgacctcctacccaaggagggaaacgggttttattggtttcttaacaacccatgtcaaa  c.2895-121

.         .         .         .         .         .           g.104696
gtaaaaattgttttgatcacctttggctgcattttcatttaatccgattgggtaagttat  c.2895-61

.         .         .         .         .         .           g.104756
ggcatcatgatgggcatggagtcagcgttctaactggctgcctttcttctctgttttaag  c.2895-1