chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 22370313 22370314 A G 7 GENIC homozygous 971458499 X 22375870 22375871 T G 6 GENIC homozygous 971458500 X 22376575 22376576 T C 13 GENIC homozygous 971458501 X 22378465 22378466 C T 12 GENIC homozygous 971458502 X 22378673 22378674 C T 9 GENIC homozygous 971458503 X 22378815 22378816 C T 16 GENIC homozygous 971458504 X 22379617 22379618 T G 12 GENIC homozygous 971458505 X 22379822 22379823 T A 13 GENIC homozygous 971458506 X 22380017 22380018 C T 5 GENIC homozygous 971458507 X 22380110 22380111 A G 9 GENIC homozygous 971458508 X 22380873 22380874 T A 15 GENIC homozygous 971458509 X 22381416 22381417 C T 19 GENIC homozygous 971458510 X 22381489 22381490 C T 19 GENIC homozygous 971458511 X 22382298 22382299 A T 13 GENIC homozygous 971458512 X 22383470 22383471 A T 7 GENIC homozygous 971458513 X 22384352 22384353 G A 17 GENIC homozygous 971458514 X 22384362 22384363 A G 17 GENIC homozygous 971458515 X 22384729 22384730 T C 21 GENIC homozygous 971458516 X 22385211 22385212 A G 17 GENIC homozygous 971458517 X 22385579 22385580 A G 18 GENIC homozygous 971458518 X 22387985 22387986 C T 8 GENIC homozygous 971458519 X 22388298 22388299 T C 11 GENIC homozygous 971458520 X 22388387 22388388 T A 13 GENIC homozygous 971458521 X 22389171 22389172 C T 15 GENIC homozygous 971458522 X 22389273 22389274 G A 9 GENIC homozygous 971458523 X 22390337 22390338 A G 11 GENIC homozygous 971458524 X 22391196 22391197 T C 17 GENIC homozygous 971458525 X 22395656 22395657 T C 14 GENIC homozygous 971458526