chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	39624902	39624903	G	A	51	GENIC	homozygous	148619454
15	39626079	39626080	A	G	30	GENIC	homozygous	139719034
15	39626218	39626219	C	T	38	GENIC	homozygous	148619455
15	39626291	39626292	C	T	40	GENIC	homozygous	148619456
15	39626323	39626324	C	A	45	GENIC	homozygous	148619457
15	39627826	39627826		TCTGTC	24	GENIC	possibly homozygous	139630386
15	39627862	39627863	A	T	28	GENIC	heterozygous	139719037
15	39629174	39629175	G	A	57	GENIC	homozygous	148619458
15	39630734	39630735	T	C	44	GENIC	homozygous	139719040
15	39630921	39630922	G	T	48	GENIC	homozygous	139719041
15	39631404	39631405	G	A	50	GENIC	homozygous	148619459
15	39640509	39640510	A	G	26	GENIC	homozygous	148619460
15	39640511	39640512	G	A	25	GENIC	homozygous	148619461
15	39640811	39640815	GGGT		20	GENIC	homozygous	148605170
15	39626229	39626230	G		37	GENIC	homozygous	148605167
15	39626243	39626246	TTC		31	GENIC	homozygous	148605168
15	39640449	39640463	GTGTATGTCTGTGT		23	GENIC	homozygous	148605169
15	39641000	39641001	A	C	42	GENIC	homozygous	148619462
15	39641671	39641672	T	C	48	GENIC	homozygous	148619463
15	39642649	39642650	G	A	38	GENIC	homozygous	139719074
15	39645477	39645477		AC	35	GENIC	homozygous	148605171
15	39646864	39646865	T	C	43	GENIC	homozygous	148619464
15	39649731	39649732	A	C	43	GENIC	homozygous	139719077