chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	156220227	156220227		GTAGA	44	GENIC	homozygous	135438915
1	156222075	156222076	T	A	39	GENIC	homozygous	153879770
1	156222075	156222076	T	G	39	GENIC	heterozygous	153879771
1	156223656	156223657	T		40	GENIC	homozygous	135438917
1	156221479	156221479		TG	44	GENIC	possibly homozygous	141172458
1	156224956	156224957	A	G	49	GENIC	homozygous	135716307
1	156227742	156227743	G	A	33	GENIC	homozygous	135716310
1	156222738	156222739	T	G	38	GENIC	homozygous	135716304
1	156222758	156222759	T	C	38	GENIC	homozygous	135716305
1	156226224	156226225	G	A	31	GENIC	homozygous	135716308
1	156226430	156226431	C	T	33	GENIC	homozygous	135716309
1	156225895	156225896	G	A	40	GENIC	possibly homozygous	143793287
1	156228820	156228821	C	G	38	GENIC	homozygous	135716311
1	156233019	156233022	GCC		6	GENIC	heterozygous	135438920
1	156233716	156233716		C	3	GENIC	heterozygous	135438921
1	156234413	156234413		A	17	GENIC	heterozygous	135438924
1	156234573	156234574	C		31	GENIC	heterozygous	135438925
1	156235427	156235428	G	A	9	GENIC	possibly homozygous	141265621
1	156237957	156237957		C	41	GENIC	homozygous	135438926
1	156237978	156237979	G	T	46	GENIC	possibly homozygous	143793288
1	156235611	156235612	C	T	13	GENIC	heterozygous	402969232