chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	52200591	52200592	T	G	30	GENIC	possibly homozygous	116884953
10	52207621	52207622	G	A	91	GENIC	heterozygous	118066839
10	52207876	52207877	A	C	44	GENIC	heterozygous	117994279
10	52207884	52207885	A	C	40	GENIC	heterozygous	117994280
10	52209071	52209072	C	T	166	GENIC	heterozygous	118066840
10	52210707	52210708	C	A	23	GENIC	homozygous	116779224
10	52210713	52210714	T	A	23	GENIC	homozygous	116779226
10	52210720	52210721	T	A	23	GENIC	homozygous	116779228
10	52210728	52210729	G	A	19	GENIC	homozygous	116779230
10	52245411	52245412	A	G	27	GENIC	heterozygous	117994295
10	52254676	52254677	T	G	19	GENIC	homozygous	117994298
10	52254785	52254786	T	A	15	GENIC	homozygous	117994299
10	52254819	52254820	C	A	25	GENIC	homozygous	117994300
10	52254939	52254940	C	T	14	GENIC	homozygous	118038023
10	52276173	52276174	A	C	17	GENIC	homozygous	116596320
10	52276207	52276208	A	C	15	GENIC	homozygous	116596322
10	52279645	52279646	C	G	74	GENIC	heterozygous	118066841
10	52284122	52284123	T	G	21	GENIC	homozygous	117328287
10	52284208	52284209	G	A	34	GENIC	homozygous	116596336
10	52272177	52272178	T	C	25	GENIC	homozygous	116933573