chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	120625392	120625393	G	A	9	GENIC	homozygous	108421285
X	120625488	120625489	T	A	9	GENIC	homozygous	108320557
X	120625906	120625907	G	T	9	GENIC	homozygous	108421287
X	120626025	120626026	A	C	4	GENIC	homozygous	108421290
X	120626300	120626301	T	C	5	GENIC	homozygous	108421292
X	120627353	120627354	C	G	6	GENIC	homozygous	108421294
X	120628572	120628573	A	T	16	GENIC	homozygous	108421296
X	120629261	120629262	T	G	2	GENIC	homozygous	108421298
X	120629267	120629268	T	G	2	GENIC	homozygous	108421300
X	120630143	120630144	C	T	7	GENIC	homozygous	108421302
X	120630284	120630285	C	A	15	GENIC	homozygous	108421304
X	120630745	120630746	A	C	11	GENIC	homozygous	108421306
X	120630844	120630845	A	G	11	GENIC	homozygous	108421308
X	120631462	120631463	G	A	12	GENIC	homozygous	108421310
X	120631530	120631531	T	C	11	GENIC	homozygous	108421312
X	120632615	120632616	A	G	8	GENIC	homozygous	108421314
X	120633059	120633060	A	G	8	GENIC	homozygous	108421316
X	120633301	120633302	C	T	3	GENIC	homozygous	108421318
X	120634237	120634238	C	A	9	GENIC	homozygous	108421320
X	120634333	120634334	C	T	9	GENIC	homozygous	108421322
X	120636291	120636292	G	A	7	GENIC	homozygous	108421324
X	120636323	120636324	T	A	9	GENIC	homozygous	108421326
X	120636899	120636900	C	A	7	GENIC	homozygous	108421328
X	120637018	120637019	G	C	6	GENIC	homozygous	108421330
X	120637794	120637795	G	A	10	GENIC	homozygous	108421332
X	120637959	120637960	T	C	15	GENIC	homozygous	108421334
X	120640919	120640920	A	G	9	GENIC	homozygous	108421342
X	120638729	120638731	AA		3	GENIC	homozygous	131243522
X	120639633	120639633		AAG	4	GENIC	homozygous	131243523
X	120638350	120638351	A	C	19	GENIC	homozygous	108421336
X	120638623	120638624	T	C	7	GENIC	homozygous	108421338
X	120640193	120640194	A	C	10	GENIC	homozygous	108421340
X	120642747	120642747		A	13	GENIC	homozygous	131243524
X	120647403	120647404	C	A	12	GENIC	homozygous	108421344
X	120644576	120644577	A	T	13	GENIC	homozygous	108454368