chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91419523	91419524	C	T	15	GENIC	possibly homozygous	116822224
10	91419786	91419787	A	G	18	GENIC	homozygous	116677429
10	91427528	91427529	T	G	13	GENIC	homozygous	116677449
10	91427657	91427658	T	C	16	GENIC	homozygous	116822226
10	91428140	91428141	G	C	30	GENIC	homozygous	116677451
10	91430064	91430065	C	T	26	GENIC	homozygous	116677455
10	91430486	91430487	G	A	14	GENIC	homozygous	116677457
10	91439055	91439056	A	C	37	GENIC	homozygous	116677461
10	91439517	91439518	G	C	26	GENIC	homozygous	116677463
10	91440185	91440186	A	G	20	GENIC	homozygous	116677469
10	91440333	91440334	G	A	29	GENIC	homozygous	116677471
10	91440439	91440440	A	T	29	GENIC	homozygous	116822234
10	91440547	91440548	A	G	37	GENIC	possibly homozygous	116822236
10	91441375	91441376	A	T	11	GENIC	possibly homozygous	116951918
10	91441593	91441594	C	T	10	GENIC	homozygous	116677474
10	91442107	91442108	C	T	26	GENIC	homozygous	116677476
10	91443777	91443778	C	A	22	GENIC	homozygous	116905763
10	91447211	91447212	G	A	22	GENIC	possibly homozygous	116951920
10	91449925	91449926	G	A	16	GENIC	homozygous	116677490
10	91450277	91450278	C	T	36	GENIC	homozygous	116677492