chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 15675622 15675623 C CT 45 GENIC heterozygous 60635147 1 15675630 15675632 CA -- 44 GENIC heterozygous 62479207 1 15675869 15675870 C T 22 GENIC possibly homozygous 62608129 1 15675946 15675947 T TTTC 31 GENIC heterozygous 60635155 1 15676025 15676026 T TCATCAGC 31 GENIC heterozygous 60635156 1 15676663 15676664 C T 12 GENIC homozygous 62667286 1 15676758 15676759 C T 19 GENIC homozygous 62667287 1 15676922 15676923 T TGTGA 36 GENIC homozygous 62608130 1 15676962 15676963 A C 27 GENIC homozygous 62667288 1 15677059 15677060 T C 24 GENIC possibly homozygous 62667289 1 15677405 15677406 T C 31 GENIC homozygous 62667290 1 15677528 15677529 A G 24 GENIC homozygous 62667291 1 15677644 15677645 C G 26 GENIC homozygous 62667292 1 15678037 15678038 A - 18 GENIC homozygous 62667293 1 15678283 15678284 C T 21 GENIC homozygous 62667294 1 15679295 15679296 G A 18 GENIC homozygous 62667295 1 15679884 15679885 G A 43 GENIC homozygous 62667296 1 15679891 15679892 C T 41 GENIC homozygous 62667297 1 15680019 15680020 C T 26 GENIC homozygous 62667298 1 15680050 15680051 C T 28 GENIC homozygous 62667299 1 15680146 15680147 C T 27 GENIC homozygous 62667300 1 15680373 15680374 A ATT 11 GENIC possibly homozygous 62667301 1 15680439 15680440 A T 18 GENIC homozygous 62608132 1 15680566 15680567 C A 15 GENIC homozygous 62667302