chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	95299258	95299259	A	T	33	GENIC	homozygous	145284344
1	95300614	95300615	C	T	35	GENIC	homozygous	145284345
1	95301543	95301544	C		7	GENIC	heterozygous	147729834
1	95301543	95301544	C	T	7	GENIC	possibly homozygous	403795207
1	95301573	95301574	A	G	13	GENIC	homozygous	145284346
1	95301660	95301661	A	G	26	GENIC	homozygous	145284347
1	95301772	95301773	G	T	39	GENIC	homozygous	145284348
1	95303845	95303846	T	C	44	GENIC	homozygous	145284349
1	95304521	95304522	G	A	41	GENIC	homozygous	145284350
1	95307430	95307431	A	G	21	GENIC	homozygous	145284351
1	95307691	95307692	T	C	38	GENIC	homozygous	145284352
1	95307713	95307714	G	A	38	GENIC	homozygous	145284353
1	95305564	95305565	C		32	GENIC	homozygous	145237087
1	95307904	95307908	CAAA		21	GENIC	homozygous	145237089
1	95301979	95301979		CCTGGGCCCCACAGGTGCCCTTTTTTATTTTTGAAACAGTATGCCATGTTGCAGTG	24	GENIC	homozygous	145237085
1	95305506	95305510	TTTG		29	GENIC	homozygous	145237086
1	95306628	95306629	G		44	GENIC	homozygous	145237088
1	95309716	95309717	A	C	37	GENIC	homozygous	145284354
1	95309925	95309925		CTAT	31	GENIC	homozygous	145237090
1	95309975	95309976	G	A	23	GENIC	homozygous	145284355
1	95310389	95310390	A	C	37	GENIC	homozygous	145284356
1	95310932	95310933	G	T	22	GENIC	homozygous	145284357
1	95310933	95310934	C	T	23	GENIC	homozygous	145284358
1	95311804	95311805	G	A	28	GENIC	homozygous	145284359
1	95311893	95311894	T	C	35	GENIC	homozygous	145284360
1	95312833	95312834	C	T	28	GENIC	homozygous	145284361
1	95314785	95314786	G	A	37	GENIC	homozygous	145284362