chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 6557017 6557018 T A 23 GENIC homozygous 108219743 X 6558301 6558302 C G 39 GENIC homozygous 108219745 X 6559089 6559090 G A 43 GENIC homozygous 108219747 X 6562629 6562630 A T 31 GENIC homozygous 108219749 X 6566431 6566432 T C 48 GENIC homozygous 108219751 X 6571215 6571216 A G 33 GENIC homozygous 108219753 X 6577193 6577194 A T 22 GENIC homozygous 108219755 X 6577570 6577571 A T 28 GENIC homozygous 108219757 X 6578442 6578443 A T 24 GENIC homozygous 108219759 X 6562539 6562539 A 28 GENIC homozygous 129717661 X 6570967 6570967 C 30 GENIC homozygous 129717662 X 6573162 6573162 T 24 GENIC homozygous 129717663 X 6573165 6573165 T 24 GENIC possibly homozygous 129717664 X 6573658 6573658 T 8 GENIC homozygous 129717665 X 6579342 6579347 GTATG 33 GENIC homozygous 129717666 X 6583184 6583185 G 12 GENIC possibly homozygous 129717667 X 6583186 6583189 TAG 12 GENIC possibly homozygous 129717668 X 6573052 6573053 A G 7 GENIC homozygous 119983717 X 6585493 6585494 A 29 GENIC homozygous 129717669 X 6585621 6585622 T C 25 GENIC homozygous 119901820 X 6589306 6589307 G A 22 GENIC homozygous 108219761 X 6589455 6589456 T 27 GENIC homozygous 129717670 X 6596237 6596237 G 12 GENIC heterozygous 129717671 X 6598539 6598540 C T 20 GENIC homozygous 108219763 X 6602277 6602278 G T 30 GENIC homozygous 108219765 X 6602283 6602284 G T 29 GENIC homozygous 108219767 X 6602287 6602288 T 28 GENIC homozygous 129717673 X 6605522 6605522 A 21 GENIC heterozygous 133452984 X 6607251 6607252 C 25 GENIC homozygous 129717674 X 6615262 6615263 T 27 GENIC homozygous 129717676