chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	93909218	93909219	A	G	30	GENIC	homozygous	111958108
3	93909512	93909513	T	C	33	GENIC	homozygous	112134396
3	93910676	93910677	A	G	29	GENIC	homozygous	111958110
3	93912391	93912392	A	C	22	GENIC	homozygous	111958114
3	93912523	93912524	A	G	19	GENIC	homozygous	111958116
3	93912584	93912585	T	C	22	GENIC	homozygous	111958118
3	93913801	93913802	C	T	20	GENIC	homozygous	112134397
3	93917565	93917566	A	G	23	GENIC	homozygous	112134398
3	93919695	93919696	T	C	28	GENIC	homozygous	111958126
3	93920274	93920275	T	C	16	GENIC	homozygous	112134399
3	93921882	93921883	T	C	25	GENIC	possibly homozygous	112255187
3	93922211	93922212	T	C	32	GENIC	homozygous	112134400
3	93922887	93922888	A	G	29	GENIC	homozygous	112134401
3	93923613	93923614	A	G	15	GENIC	homozygous	112134402
3	93923758	93923759	G	A	18	GENIC	homozygous	112134403
3	93924138	93924139	G	T	25	GENIC	possibly homozygous	112134404
3	93924763	93924764	A	T	14	GENIC	homozygous	112134405
3	93925103	93925104	G	A	33	GENIC	homozygous	112134406
3	93925688	93925689	G	T	18	GENIC	homozygous	112134407
3	93927394	93927395	C	T	22	GENIC	homozygous	112134408
3	93927687	93927688	G	A	24	GENIC	homozygous	111958140
3	93928745	93928746	C	G	25	GENIC	homozygous	112134409
3	93928992	93928993	C	T	34	GENIC	homozygous	112134410
3	93929432	93929433	G	A	29	GENIC	homozygous	112134411
3	93929668	93929669	C	T	27	GENIC	homozygous	112134412
3	93929732	93929733	C	A	31	GENIC	homozygous	112134413
3	93929756	93929757	A	G	30	GENIC	homozygous	112134414
3	93930346	93930347	G	A	25	GENIC	possibly homozygous	112134415
3	93930983	93930984	C	T	27	GENIC	homozygous	112134416
3	93931187	93931188	G	C	31	GENIC	homozygous	112134417