chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	113703045	113703046	A	T	17	GENIC	homozygous	154544153
8	113703045	113703046	A		17	GENIC	heterozygous	403250068
8	113713648	113713649	A	T	24	GENIC	homozygous	138421375
8	113727122	113727123	A	C	17	GENIC	homozygous	138421376
8	113729148	113729149	G	A	16	GENIC	homozygous	138421377
8	113729797	113729798	G	A	17	GENIC	homozygous	138421378
8	113729853	113729854	T	C	15	GENIC	homozygous	138421379
8	113782415	113782416	G		15	GENIC	possibly homozygous	403250069
8	113782415	113782416	G	C	15	GENIC	heterozygous	403250070
8	113782415	113782416	G	T	15	GENIC	heterozygous	403250071
8	113782417	113782418	G		15	GENIC	possibly homozygous	403250072
8	113782417	113782418	G	C	15	GENIC	heterozygous	403250073
8	113782417	113782418	G	T	15	GENIC	heterozygous	403250074
8	113782419	113782420	G		15	GENIC	possibly homozygous	403250075
8	113782419	113782420	G	C	15	GENIC	heterozygous	403250076
8	113782421	113782422	G		15	GENIC	possibly homozygous	403250077
8	113782421	113782422	G	C	15	GENIC	heterozygous	403250078
8	113782423	113782424	G		15	GENIC	possibly homozygous	403250079
8	113782423	113782424	G	C	15	GENIC	heterozygous	403250080
8	113799907	113799908	C	T	30	GENIC	homozygous	138421381
8	113769169	113769170	C	G	10	GENIC	heterozygous	142103542
8	113741838	113741839	T		31	GENIC	homozygous	138265953
8	113729561	113729561		T	15	GENIC	heterozygous	144047180
8	113729898	113729899	T		19	GENIC	homozygous	138265951
8	113733048	113733050	GT		10	GENIC	heterozygous	138265952
8	113847491	113847492	G	C	14	GENIC	homozygous	138421383
8	113853778	113853779	C	T	30	GENIC	homozygous	138421384
8	113845083	113845083		TGGA	16	GENIC	homozygous	148529402