chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	108985490	108985491	C	T	58	GENIC	homozygous	136786072
3	108987893	108987893		T	62	GENIC	homozygous	136583224
3	108988032	108988033	C	G	41	GENIC	homozygous	136786073
3	108988217	108988218	A	C	69	GENIC	homozygous	136786074
3	108988282	108988283	T	C	69	GENIC	homozygous	136786075
3	108989468	108989469	T	A	57	GENIC	homozygous	136786076
3	108989916	108989924	TTTTTTTC		9	GENIC	heterozygous	136583225
3	108990163	108990164	G	A	60	GENIC	homozygous	136786077
3	108991002	108991003	T	C	61	GENIC	homozygous	136786078
3	108991072	108991073	C	T	61	GENIC	homozygous	136786079
3	108991672	108991673	C	T	59	GENIC	homozygous	136786080
3	108992347	108992351	AAAT		50	GENIC	homozygous	136583226
3	108992434	108992435	G	A	62	GENIC	homozygous	136786081
3	108993315	108993316	T	C	51	GENIC	homozygous	136786082
3	108993678	108993679	T	A	75	GENIC	homozygous	136786083
3	108993948	108993949	G	A	65	GENIC	homozygous	136786084
3	108995644	108995645	C	T	72	GENIC	homozygous	136786085
3	108995964	108995965	G	A	50	GENIC	homozygous	136786086
3	108996527	108996527		TGT	54	GENIC	homozygous	136583227
3	108997103	108997104	A	C	63	GENIC	homozygous	136786087
3	108997894	108997895	C		49	GENIC	homozygous	136583228
3	108998067	108998068	G	T	40	GENIC	homozygous	136786088
3	108999516	108999517	A	C	49	GENIC	homozygous	136786089
3	109000260	109000261	T	C	52	GENIC	homozygous	136786090
3	109000553	109000559	TTGACC		59	GENIC	homozygous	136583229
3	109000578	109000579	T	C	60	GENIC	homozygous	136786091
3	109000621	109000622	A	T	48	GENIC	homozygous	136786092
3	109001603	109001604	G	A	61	GENIC	homozygous	136786093
3	109001994	109001995	C	T	59	GENIC	homozygous	136786094
3	109002825	109002826	A		44	GENIC	homozygous	136583230
3	109002884	109002885	A	G	40	GENIC	homozygous	136786095
3	109003294	109003295	T	C	38	GENIC	homozygous	136786096
3	109005511	109005512	G	A	67	GENIC	homozygous	136786097
3	109006238	109006239	G	A	53	GENIC	possibly homozygous	136786098