chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	57065892	57065893	A	G	20	GENIC	homozygous	116784925
10	57066118	57066119	T	C	16	GENIC	homozygous	116784927
10	57066165	57066166	C	T	19	GENIC	homozygous	116603127
10	57066641	57066642	C	T	22	GENIC	homozygous	117060095
10	57066812	57066813	A	G	29	GENIC	homozygous	117060097
10	57067570	57067571	T	C	21	GENIC	homozygous	117060105
10	57067726	57067727	G	T	30	GENIC	homozygous	117060107
10	57067856	57067857	T	G	33	GENIC	homozygous	117060109
10	57067891	57067892	T	C	39	GENIC	homozygous	117060111
10	57067897	57067898	C	T	39	GENIC	homozygous	117060113
10	57068051	57068052	C	T	47	GENIC	homozygous	117060115
10	57068222	57068223	C	A	29	GENIC	homozygous	117060117
10	57068251	57068252	A	G	32	GENIC	homozygous	117060119
10	57068319	57068320	C	T	24	GENIC	homozygous	117060121
10	57068351	57068352	T	G	26	GENIC	homozygous	117060123
10	57068403	57068404	C	T	27	GENIC	homozygous	117060125
10	57068566	57068567	T	C	32	GENIC	homozygous	117060127
10	57068614	57068615	T	G	27	GENIC	homozygous	117060129
10	57068741	57068742	C	T	34	GENIC	homozygous	117060131
10	57068818	57068819	T	A	30	GENIC	homozygous	117060133
10	57068835	57068836	G	C	29	GENIC	homozygous	117078907
10	57068836	57068837	T	A	30	GENIC	homozygous	117060135
10	57068979	57068980	A	G	32	GENIC	homozygous	117060137
10	57069313	57069314	C	T	31	GENIC	homozygous	116784933
10	57069787	57069788	G	A	17	GENIC	homozygous	116784937
10	57070409	57070410	G	T	17	GENIC	homozygous	117078908
10	57070428	57070429	G	A	18	GENIC	homozygous	117078909
10	57070670	57070671	C	T	24	GENIC	homozygous	117060139
10	57070697	57070698	A	T	21	GENIC	homozygous	117060141
10	57070742	57070743	G	A	18	GENIC	homozygous	117060143
10	57070862	57070863	C	G	8	GENIC	homozygous	117060145
10	57070972	57070973	G	C	11	GENIC	homozygous	117060147