chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10135975	10135976	C	G	32	GENIC	homozygous	110953758
17	10135983	10135984	G	A	36	GENIC	homozygous	110953760
17	10136958	10136959	A	G	14	GENIC	homozygous	110953762
17	10139153	10139154	G	A	28	GENIC	homozygous	111230470
17	10141684	10141685	G	C	20	GENIC	homozygous	110953772
17	10146647	10146648	G	A	45	GENIC	homozygous	111230472
17	10148778	10148779	T	C	20	GENIC	homozygous	111230474
17	10149033	10149034	T	C	21	GENIC	homozygous	110953786
17	10149320	10149321	G	T	32	GENIC	homozygous	110953788
17	10149389	10149390	C	G	25	GENIC	homozygous	110953790
17	10149419	10149420	G	T	26	GENIC	homozygous	110953794
17	10149499	10149500	A	G	22	GENIC	homozygous	110953796
17	10149555	10149556	C	T	24	GENIC	homozygous	110953798
17	10149610	10149611	G	C	25	GENIC	homozygous	110953800
17	10150359	10150360	G	A	36	GENIC	homozygous	110953802
17	10150389	10150390	A	G	19	GENIC	homozygous	110953804
17	10150739	10150740	G	A	13	GENIC	homozygous	110953806
17	10150806	10150807	C	T	29	GENIC	homozygous	110953808
17	10150886	10150887	T	C	22	GENIC	homozygous	110953810
17	10151060	10151061	T	G	16	GENIC	homozygous	110953813
17	10151216	10151217	T	C	14	GENIC	homozygous	110953815
17	10151291	10151292	A	G	24	GENIC	homozygous	110953817
17	10151338	10151339	G	T	24	GENIC	homozygous	110953819
17	10151415	10151416	A	G	38	GENIC	homozygous	110953821
17	10151499	10151500	G	T	33	GENIC	homozygous	110953823
17	10151589	10151590	A	G	34	GENIC	homozygous	110953825
17	10151698	10151699	A	G	35	GENIC	homozygous	110953827
17	10151801	10151802	G	A	30	GENIC	homozygous	110953829
17	10152211	10152212	G	T	30	GENIC	homozygous	110953831
17	10152324	10152325	T	C	24	GENIC	homozygous	110953833