chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	61853245	61853246	G	A	31	GENIC	homozygous	112670633
4	61853267	61853268	T	C	37	GENIC	homozygous	112670635
4	61853613	61853614	A	C	44	GENIC	homozygous	112670637
4	61854623	61854624	G	A	33	GENIC	homozygous	112670639
4	61854860	61854861	A	G	53	GENIC	homozygous	112670641
4	61857238	61857239	C	T	51	GENIC	homozygous	112670643
4	61857481	61857482	C	T	57	GENIC	homozygous	112670645
4	61858170	61858171	C	G	39	GENIC	homozygous	112670647
4	61858944	61858945	C	T	40	GENIC	homozygous	112670649
4	61859874	61859875	G	A	46	GENIC	homozygous	112670651
4	61861064	61861065	C	A	53	GENIC	possibly homozygous	112670653
4	61861316	61861317	C	A	40	GENIC	homozygous	112670655
4	61862353	61862354	T	C	42	GENIC	homozygous	112670657
4	61863269	61863270	C	T	47	GENIC	possibly homozygous	112670659
4	61863757	61863758	C	G	32	GENIC	homozygous	112670661
4	61864097	61864098	T	C	40	GENIC	homozygous	112670663
4	61866352	61866353	G	A	37	GENIC	homozygous	112670666
4	61866757	61866758	C	T	33	GENIC	homozygous	112670668
4	61867074	61867075	C	T	46	GENIC	homozygous	112670670
4	61870763	61870764	G	A	49	GENIC	homozygous	112670678
4	61867479	61867480	T	C	33	GENIC	possibly homozygous	112670672
4	61867493	61867494	C	T	30	GENIC	possibly homozygous	112670674
4	61870570	61870571	C	T	28	GENIC	homozygous	112670676
4	61870946	61870947	C	G	56	GENIC	homozygous	112670680
4	61871130	61871131	T	A	37	GENIC	homozygous	112670682
4	61874422	61874423	A	G	50	GENIC	homozygous	112670684
4	61876369	61876370	A	T	37	GENIC	homozygous	112670686
4	61877232	61877233	A	G	52	GENIC	homozygous	112670688
4	61877392	61877393	A	G	61	GENIC	homozygous	112670690
4	61877887	61877888	C	T	27	GENIC	homozygous	112670692
4	61878263	61878264	A	C	29	GENIC	homozygous	112670694
4	61878743	61878744	T	A	67	GENIC	possibly homozygous	112670696