chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	80893184	80893185	T	C	23	GENIC	homozygous	111635909
3	80893198	80893199	G	T	22	GENIC	homozygous	111635910
3	80893743	80893744	C	T	27	GENIC	homozygous	111635911
3	80894023	80894024	T	C	22	GENIC	homozygous	111635912
3	80894312	80894313	G	A	22	GENIC	homozygous	112242174
3	80894858	80894859	T	C	20	GENIC	homozygous	111635914
3	80894871	80894872	T	C	21	GENIC	homozygous	111635915
3	80895564	80895565	C	G	21	GENIC	homozygous	112242175
3	80895990	80895991	G	A	31	GENIC	homozygous	111635916
3	80897140	80897141	T	C	34	GENIC	homozygous	111635917
3	80897591	80897592	A	T	17	GENIC	homozygous	111635918
3	80897613	80897614	T	G	21	GENIC	homozygous	112242176
3	80906838	80906839	T	C	30	GENIC	homozygous	111635921
3	80906896	80906897	C	T	35	GENIC	heterozygous	112242177
3	80907360	80907361	C	T	45	GENIC	heterozygous	111635922
3	80908685	80908686	A	G	44	GENIC	homozygous	111635923
3	80910171	80910172	T	C	16	GENIC	homozygous	111950754
3	80911174	80911175	G	A	25	GENIC	homozygous	112242178
3	80912340	80912341	A	G	18	GENIC	homozygous	111950758
3	80914521	80914522	T	A	17	GENIC	homozygous	111950762
3	80914688	80914689	A	T	16	GENIC	homozygous	111635927
3	80916047	80916048	T	G	26	GENIC	homozygous	112242179
3	80919599	80919600	A	G	28	GENIC	possibly homozygous	111635929
3	80922107	80922108	C	T	18	GENIC	homozygous	111950766
3	80923279	80923280	C	G	30	GENIC	homozygous	111635930
3	80925777	80925778	T	C	40	GENIC	homozygous	112242180
3	80932753	80932754	T	G	14	GENIC	homozygous	111950774
3	80929669	80929670	C	G	4	GENIC	homozygous	119797082