chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 22370313 22370314 A G 8 GENIC homozygous 956815046 X 22372661 22372662 C T 21 GENIC homozygous 956815047 X 22375870 22375871 T G 14 GENIC homozygous 956815048 X 22376575 22376576 T C 11 GENIC homozygous 956815049 X 22378465 22378466 C T 11 GENIC homozygous 956815050 X 22378673 22378674 C T 4 GENIC homozygous 956815051 X 22378815 22378816 C T 5 GENIC homozygous 956815052 X 22379617 22379618 T G 14 GENIC homozygous 956815053 X 22379822 22379823 T A 12 GENIC possibly homozygous 956815054 X 22380110 22380111 A G 7 GENIC homozygous 956815055 X 22380873 22380874 T A 14 GENIC homozygous 956815056 X 22381416 22381417 C T 6 GENIC homozygous 956815057 X 22381489 22381490 C T 8 GENIC homozygous 956815058 X 22382298 22382299 A T 8 GENIC homozygous 956815059 X 22383470 22383471 A T 10 GENIC homozygous 956815060 X 22384352 22384353 G A 15 GENIC homozygous 956815061 X 22384362 22384363 A G 16 GENIC homozygous 956815062 X 22384729 22384730 T C 6 GENIC homozygous 956815063 X 22385211 22385212 A G 10 GENIC homozygous 956815064 X 22385579 22385580 A G 14 GENIC homozygous 956815065 X 22387985 22387986 C T 6 GENIC homozygous 956815066 X 22388298 22388299 T C 10 GENIC homozygous 956815067 X 22388387 22388388 T A 12 GENIC homozygous 956815068 X 22389171 22389172 C T 7 GENIC homozygous 956815069 X 22389273 22389274 G A 14 GENIC homozygous 956815070 X 22390337 22390338 A G 21 GENIC homozygous 956815071