chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	155649440	155649441	A	G	19	GENIC	homozygous	114065266
5	155651953	155651954	A	C	54	GENIC	possibly homozygous	114065268
5	155652202	155652203	G	A	32	GENIC	heterozygous	114065270
5	155652206	155652207	G	A	37	GENIC	heterozygous	114065272
5	155652258	155652259	A	G	43	GENIC	heterozygous	114065274
5	155652728	155652729	T	C	38	GENIC	homozygous	114065276
5	155653027	155653028	T	C	42	GENIC	homozygous	114065278
5	155653479	155653480	T	C	50	GENIC	homozygous	114065280
5	155654652	155654653	C	T	35	GENIC	homozygous	114065282
5	155654702	155654703	G	A	32	GENIC	homozygous	114065284
5	155655005	155655006	G	A	48	GENIC	homozygous	114065286
5	155656064	155656065	T	C	53	GENIC	heterozygous	114065288
5	155656068	155656069	T	C	50	GENIC	heterozygous	114065290
5	155656076	155656077	C	T	61	GENIC	heterozygous	114159013
5	155656092	155656093	C	T	54	GENIC	heterozygous	114159014
5	155657740	155657741	G	A	29	GENIC	possibly homozygous	114065292
5	155658318	155658319	G	A	41	GENIC	homozygous	114065294
5	155658727	155658728	G	A	50	GENIC	possibly homozygous	114065296
5	155659324	155659325	T	G	26	GENIC	heterozygous	114651813
5	155659467	155659468	A	G	46	GENIC	homozygous	114065298
5	155660735	155660736	T	C	39	GENIC	homozygous	114065300
5	155663226	155663227	C	T	45	GENIC	homozygous	114065302
5	155664156	155664157	A	G	46	GENIC	homozygous	114065304
5	155665515	155665516	T	C	31	GENIC	homozygous	114065306
5	155665649	155665650	T	G	38	GENIC	homozygous	114065308
5	155665765	155665766	A	G	52	GENIC	homozygous	114065310
5	155666217	155666218	G	A	41	GENIC	homozygous	114065312
5	155667390	155667391	T	C	42	GENIC	homozygous	114065314