chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 51509489 51509490 A 32 GENIC heterozygous 130392590 10 51548782 51548783 A C 55 GENIC homozygous 116594416 10 51554657 51554657 G 36 GENIC homozygous 128817098 10 51559600 51559601 A T 25 GENIC heterozygous 132696294 10 51561007 51561008 T C 18 GENIC homozygous 123358740 10 51561007 51561007 C 17 GENIC homozygous 128817103 10 51561010 51561015 TGTTA 18 GENIC homozygous 128817104 10 51561017 51561017 TAGG 19 GENIC homozygous 128817105 10 51561020 51561022 AA 18 GENIC homozygous 128817106 10 51561026 51561027 G C 16 GENIC homozygous 123358745 10 51561028 51561029 T C 16 GENIC homozygous 123358746 10 51586004 51586005 C A 19 GENIC possibly homozygous 117994137 10 51594207 51594207 C 9 GENIC homozygous 128817118 10 51594212 51594213 G 12 GENIC homozygous 128817119 10 51594260 51594262 GC 15 GENIC homozygous 128817120 10 51594295 51594295 A 25 GENIC homozygous 128817121 10 51594299 51594299 G 26 GENIC homozygous 128817122 10 51594372 51594372 T 32 GENIC homozygous 128817123 10 51594379 51594379 T 33 GENIC homozygous 128817124 10 51594446 51594446 T 34 GENIC homozygous 128817125 10 51594468 51594469 G A 30 GENIC homozygous 116594522 10 51594480 51594480 A 32 GENIC homozygous 128817126 10 51594507 51594507 T 27 GENIC homozygous 128817127 10 51594517 51594517 C 25 GENIC homozygous 128817128 10 51561070 51561071 G A 15 GENIC homozygous 117078291 10 51656353 51656353 C 51 GENIC homozygous 128817148 10 51657396 51657396 C 50 GENIC homozygous 128817149 10 51657400 51657400 AC 49 GENIC homozygous 128817150 10 51657408 51657409 C 46 GENIC homozygous 128817151 10 51657530 51657530 TGT 37 GENIC homozygous 128817152 10 51657684 51657684 C 7 GENIC homozygous 129969015 10 51657527 51657528 C G 37 GENIC homozygous 116884939