chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	151752995	151752996	T	C	48	GENIC	homozygous	71220005
4	151753089	151753090	A	G	40	GENIC	homozygous	71220008
4	151753484	151753485	C	T	30	GENIC	possibly homozygous	71220011
4	151753518	151753519	G	T	26	GENIC	heterozygous	71220014
4	151753805	151753806	T	C	66	GENIC	homozygous	71220017
4	151754161	151754162	T	G	52	GENIC	homozygous	71220020
4	151754958	151754959	A	G	49	GENIC	homozygous	71220023
4	151755214	151755215	T	C	54	GENIC	homozygous	71220025
4	151755420	151755421	G	A	47	GENIC	homozygous	71220028
4	151756412	151756413	G	T	25	GENIC	homozygous	71220031
4	151758256	151758257	A	G	64	GENIC	homozygous	71220034
4	151760501	151760502	A	G	47	GENIC	homozygous	71220037
4	151761359	151761360	T	C	53	GENIC	possibly homozygous	71220040
4	151762544	151762545	T	G	27	GENIC	homozygous	71220043
4	151762778	151762779	C	T	31	GENIC	homozygous	71220046
4	151764650	151764651	C	T	35	GENIC	homozygous	71220049
4	151765080	151765081	C	T	37	GENIC	homozygous	71220052
4	151765510	151765511	A	G	56	GENIC	homozygous	71220055
4	151765688	151765689	T	C	46	GENIC	homozygous	71220058
4	151765775	151765776	T	A	49	GENIC	homozygous	71220061
4	151765837	151765838	T	C	57	GENIC	homozygous	71220064
4	151766136	151766137	G	A	53	GENIC	homozygous	71220067
4	151767351	151767352	G	A	40	GENIC	homozygous	71220070
4	151767902	151767903	G	A	41	GENIC	homozygous	71220073
4	151768138	151768139	C	T	33	GENIC	homozygous	71220076
4	151769231	151769232	T	C	63	GENIC	homozygous	71220079
4	151769601	151769602	T	C	25	GENIC	homozygous	71220082
4	151769765	151769766	C	T	21	GENIC	homozygous	71220085
4	151770373	151770374	A	G	60	GENIC	homozygous	71220087
4	151770438	151770439	G	A	58	GENIC	homozygous	71220090
4	151771512	151771513	G	A	50	GENIC	homozygous	71220093
4	151772177	151772178	T	C	24	GENIC	homozygous	71220096
4	151773183	151773184	C	T	23	GENIC	homozygous	71220099
4	151775307	151775308	A	C	51	GENIC	homozygous	71220102