chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	93909218	93909219	A	G	11	GENIC	homozygous	111958108
3	93910676	93910677	A	G	19	GENIC	homozygous	111958110
3	93910861	93910862	G	A	9	GENIC	homozygous	112443044
3	93910881	93910882	C	T	10	GENIC	homozygous	111958112
3	93911365	93911366	C	T	17	GENIC	homozygous	112443045
3	93912391	93912392	A	C	14	GENIC	homozygous	111958114
3	93912474	93912475	A	G	11	GENIC	homozygous	112443047
3	93912523	93912524	A	G	15	GENIC	homozygous	111958116
3	93912584	93912585	T	C	10	GENIC	homozygous	111958118
3	93913702	93913703	G	A	8	GENIC	homozygous	112443048
3	93919695	93919696	T	C	19	GENIC	homozygous	111958126
3	93927394	93927395	C	T	8	GENIC	homozygous	112134408
3	93927687	93927688	G	A	9	GENIC	homozygous	111958140
3	93927999	93928000	G	A	5	GENIC	homozygous	112443049
3	93928745	93928746	C	G	7	GENIC	homozygous	112134409
3	93928992	93928993	C	T	12	GENIC	homozygous	112134410
3	93929432	93929433	G	A	9	GENIC	homozygous	112134411
3	93929530	93929531	C	T	13	GENIC	homozygous	112443050
3	93929668	93929669	C	T	20	GENIC	homozygous	112134412
3	93929756	93929757	A	G	15	GENIC	homozygous	112134414
3	93930346	93930347	G	A	9	GENIC	homozygous	112134415
3	93931333	93931334	A	T	10	GENIC	homozygous	119683466
3	93931334	93931335	G	A	10	GENIC	homozygous	119683468
3	93931657	93931658	T	A	12	GENIC	homozygous	119683470
3	93931658	93931659	A	G	12	GENIC	homozygous	119683472
3	93931874	93931875	A	T	7	GENIC	homozygous	119683474
3	93931887	93931888	A	C	7	GENIC	homozygous	119683476