chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	193565485	193565486	C	T	34	GENIC	homozygous	110183247
2	193566100	193566101	G	C	33	GENIC	homozygous	110183248
2	193567766	193567767	A	T	14	GENIC	heterozygous	120298427
2	193567836	193567837	G	A	26	GENIC	homozygous	110183249
2	193568437	193568438	C	T	45	GENIC	homozygous	110183250
2	193569902	193569903	C	T	40	GENIC	homozygous	110183251
2	193570627	193570628	T	C	38	GENIC	homozygous	110183252
2	193571976	193571977	G	C	31	GENIC	homozygous	110183257
2	193569914	193569915	T		40	GENIC	homozygous	127720741
2	193571702	193571703	T	C	40	GENIC	possibly homozygous	110183253
2	193571809	193571810	C	G	34	GENIC	possibly homozygous	110183254
2	193571818	193571819	A	G	33	GENIC	possibly homozygous	110183255
2	193571853	193571854	A	T	23	GENIC	homozygous	110183256
2	193572084	193572085	G	A	40	GENIC	possibly homozygous	110183258
2	193573080	193573081	C	G	853	GENIC	heterozygous	110183259
2	193573292	193573293	C	G	784	GENIC	heterozygous	110183260
2	193573338	193573338		G	656	GENIC	homozygous	127720742
2	193573484	193573484		C	80	GENIC	possibly homozygous	127720743
2	193573487	193573487		G	80	GENIC	heterozygous	134269886
2	193573542	193573542		C	16	GENIC	homozygous	127720746
2	193573607	193573608	C		88	GENIC	homozygous	127720747
2	193573712	193573712		T	45	GENIC	homozygous	127720748
2	193573714	193573715	C	G	44	GENIC	homozygous	110616231