chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	71098069	71098069		G	19	GENIC	homozygous	128602306
8	71098072	71098073	T	C	18	GENIC	homozygous	117917402
8	71098073	71098074	C	T	18	GENIC	homozygous	117917403
8	71098079	71098080	G	A	16	GENIC	homozygous	117917404
8	71098084	71098084		A	13	GENIC	homozygous	128602307
8	71098092	71098093	G		10	GENIC	homozygous	128602308
8	71098098	71098099	G		8	GENIC	homozygous	128602309
8	71098101	71098102	A		7	GENIC	homozygous	128602310
8	71098103	71098105	CA		5	GENIC	homozygous	128602311
8	71098558	71098558		A	24	GENIC	homozygous	128602312
8	71098566	71098567	C	T	22	GENIC	homozygous	122993215
8	71098567	71098568	T	C	23	GENIC	homozygous	122993216
8	71098570	71098572	CC		23	GENIC	homozygous	128602313
8	71098587	71098588	A	C	23	GENIC	homozygous	122993218
8	71098588	71098589	G	A	23	GENIC	homozygous	122993219
8	71098593	71098594	G		23	GENIC	homozygous	128602314
8	71098597	71098597		T	23	GENIC	homozygous	128602315
8	71098604	71098604		A	24	GENIC	homozygous	128602316
8	71098608	71098608		A	25	GENIC	homozygous	128602317
8	71098629	71098629		G	24	GENIC	homozygous	128602318
8	71098635	71098636	T		26	GENIC	homozygous	128602319
8	71098639	71098640	C		25	GENIC	homozygous	128602320
8	71098646	71098647	T		25	GENIC	homozygous	128602321
8	71098648	71098649	C	G	25	GENIC	homozygous	122993228
8	71098657	71098658	G	C	26	GENIC	homozygous	122993229
8	71098662	71098662		C	26	GENIC	homozygous	128602322
8	71098677	71098680	CCA		28	GENIC	homozygous	128602323
8	71098698	71098698		A	28	GENIC	homozygous	128602324
8	71099889	71099889		G	10	GENIC	homozygous	128602325
8	71099906	71099907	C		11	GENIC	homozygous	128602326
8	71103304	71103305	T		52	GENIC	homozygous	128602328
8	71103353	71103353		C	40	GENIC	homozygous	128602329
8	71103394	71103395	C		37	GENIC	homozygous	128602330
8	71103440	71103440		C	22	GENIC	homozygous	128602331
8	71099977	71099977		A	7	GENIC	homozygous	130769657