chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94191860	94191861	T	C	30	GENIC	homozygous	116684761
10	94192198	94192199	G	A	28	GENIC	homozygous	116684763
10	94193082	94193083	T	C	23	GENIC	homozygous	116684765
10	94193185	94193186	A	G	26	GENIC	homozygous	116684767
10	94193226	94193227	A	T	21	GENIC	homozygous	116684769
10	94193565	94193566	C	T	35	GENIC	homozygous	116954667
10	94193617	94193618	A	G	35	GENIC	homozygous	116684771
10	94193823	94193824	G	A	35	GENIC	possibly homozygous	116954669
10	94194310	94194311	C	G	41	GENIC	homozygous	116684773
10	94194569	94194570	G	A	33	GENIC	homozygous	116684775
10	94194998	94194999	A	G	7	GENIC	homozygous	116684777
10	94195699	94195700	G	A	33	GENIC	homozygous	116684779
10	94197819	94197820	C	T	40	GENIC	heterozygous	118051029
10	94197858	94197859	G	A	27	GENIC	heterozygous	118051032
10	94197866	94197867	G	A	29	GENIC	heterozygous	118051034
10	94197936	94197937	G	A	41	GENIC	possibly homozygous	118051038
10	94198215	94198216	C	T	30	GENIC	homozygous	116954673
10	94198320	94198321	C	T	27	GENIC	homozygous	116684815
10	94198497	94198498	A	C	6	GENIC	homozygous	117021853
10	94199109	94199110	T	C	48	GENIC	homozygous	116826128
10	94200644	94200645	G	A	42	GENIC	homozygous	116954675
10	94200980	94200981	G	A	37	GENIC	homozygous	116954677
10	94201407	94201408	T	C	11	GENIC	homozygous	116684825
10	94201664	94201665	T	C	10	GENIC	homozygous	116954679
10	94201825	94201826	C	T	31	GENIC	homozygous	116954681
10	94203028	94203029	G	T	13	GENIC	heterozygous	118009221
10	94203847	94203848	C	T	34	GENIC	homozygous	116954683
10	94204556	94204557	A	G	27	GENIC	homozygous	116954685
10	94204573	94204574	C	T	28	GENIC	homozygous	116954687
10	94205043	94205044	T	C	42	GENIC	homozygous	116684833
10	94205813	94205814	G	A	21	GENIC	homozygous	116954693
10	94198519	94198520	C	G	5	GENIC	homozygous	117088856
10	94204738	94204739	A	G	41	GENIC	homozygous	116954689
10	94205119	94205120	C	T	37	GENIC	homozygous	116954691