chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153561408 153561409 A T 14 GENIC homozygous 890098740 X 153561689 153561690 G T 10 GENIC homozygous 890098739 X 153644315 153644316 C T 13 GENIC homozygous 890098738 X 153719311 153719312 G A 4 GENIC homozygous 890098737 X 153719364 153719365 A T 12 GENIC homozygous 890098736 X 153719374 153719375 A T 7 GENIC homozygous 890098735 X 153719436 153719437 C T 6 GENIC homozygous 890098734 X 153719484 153719485 A G 4 GENIC homozygous 890098733 X 153719485 153719486 G A 4 GENIC homozygous 890098732 X 153719493 153719494 C T 5 GENIC homozygous 890098731 X 153723221 153723222 T C 9 GENIC homozygous 890098730 X 153753002 153753003 G T 4 GENIC homozygous 890098729 X 153755263 153755264 T C 9 GENIC homozygous 890098728 X 153755316 153755317 G C 19 GENIC homozygous 890098727 X 153806680 153806681 A G 5 GENIC heterozygous 890098726 X 153817525 153817526 G A 8 GENIC homozygous 890098725 X 153868287 153868288 A G 4 GENIC heterozygous 890098724 X 153890429 153890430 G A 14 GENIC homozygous 890098723 X 153913999 153914000 A G 9 GENIC heterozygous 890098722 X 153914008 153914009 A T 11 GENIC heterozygous 890098721 X 153914489 153914490 A G 11 GENIC heterozygous 890098720