chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	15294575	15294576	T	C	36	GENIC	homozygous	109651966
19	15295178	15295179	A	G	58	GENIC	homozygous	109651983
19	15304021	15304022	G	T	14	GENIC	homozygous	109652025
19	15304245	15304246	T	C	36	GENIC	homozygous	109652027
19	15304560	15304561	T	C	10	GENIC	homozygous	109652029
19	15304903	15304904	A	G	54	GENIC	homozygous	109652040
19	15305267	15305268	A	C	56	GENIC	homozygous	109652076
19	15307291	15307292	A	G	58	GENIC	homozygous	109652202
19	15307859	15307860	T	A	16	GENIC	homozygous	109652214
19	15307878	15307879	A	C	16	GENIC	homozygous	109770736
19	15308376	15308377	G	A	40	GENIC	homozygous	109652221
19	15309003	15309004	G	T	59	GENIC	homozygous	109652247
19	15309746	15309747	C	T	35	GENIC	homozygous	109652261
19	15310852	15310853	A	G	25	GENIC	homozygous	109652293
19	15310944	15310945	G	A	19	GENIC	homozygous	109652299
19	15311990	15311991	A	G	38	GENIC	homozygous	109652358
19	15326631	15326632	T	C	50	GENIC	homozygous	109850484
19	15326642	15326643	T	C	41	GENIC	heterozygous	109850486
19	15326642	15326643	T	A	41	GENIC	heterozygous	109850488
19	15329918	15329919	G	C	20	GENIC	homozygous	109770825
19	15329984	15329985	A	G	25	GENIC	homozygous	109770829
19	15333696	15333697	A	G	57	GENIC	homozygous	109652651
19	15329076	15329077	A	G	22	GENIC	homozygous	110122897