chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	93909218	93909219	A	G	76	GENIC	homozygous	111958108
3	93910676	93910677	A	G	59	GENIC	homozygous	111958110
3	93910861	93910862	G	A	65	GENIC	homozygous	112443044
3	93910881	93910882	C	T	61	GENIC	homozygous	111958112
3	93911365	93911366	C	T	52	GENIC	homozygous	112443045
3	93912391	93912392	A	C	63	GENIC	homozygous	111958114
3	93912404	93912405	G	A	63	GENIC	homozygous	112443046
3	93912474	93912475	A	G	60	GENIC	homozygous	112443047
3	93912523	93912524	A	G	54	GENIC	homozygous	111958116
3	93912584	93912585	T	C	44	GENIC	homozygous	111958118
3	93913702	93913703	G	A	56	GENIC	homozygous	112443048
3	93919695	93919696	T	C	54	GENIC	homozygous	111958126
3	93921871	93921872	G	T	50	GENIC	homozygous	111958128
3	93927394	93927395	C	T	40	GENIC	homozygous	112134408
3	93927687	93927688	G	A	46	GENIC	homozygous	111958140
3	93927999	93928000	G	A	40	GENIC	homozygous	112443049
3	93928745	93928746	C	G	49	GENIC	homozygous	112134409
3	93928992	93928993	C	T	60	GENIC	homozygous	112134410
3	93929432	93929433	G	A	39	GENIC	homozygous	112134411
3	93929530	93929531	C	T	53	GENIC	possibly homozygous	112443050
3	93929668	93929669	C	T	49	GENIC	homozygous	112134412
3	93929756	93929757	A	G	64	GENIC	homozygous	112134414
3	93930346	93930347	G	A	54	GENIC	possibly homozygous	112134415
3	93931333	93931334	A	T	48	GENIC	homozygous	119683466
3	93931334	93931335	G	A	47	GENIC	homozygous	119683468
3	93931657	93931658	T	A	60	GENIC	homozygous	119683470
3	93931658	93931659	A	G	60	GENIC	homozygous	119683472
3	93931874	93931875	A	T	36	GENIC	possibly homozygous	119683474
3	93931887	93931888	A	C	42	GENIC	homozygous	119683476
3	93917798	93917798		T	48	GENIC	homozygous	131626457
3	93921097	93921109	GCCCGCAGCATG		53	GENIC	homozygous	134193395
3	93926085	93926085		T	44	GENIC	homozygous	127909731