chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10543058	10543059	T	C	29	GENIC	homozygous	110954326
17	10543603	10543604	A	G	22	GENIC	homozygous	110954330
17	10544071	10544072	G	A	17	GENIC	homozygous	111524920
17	10544121	10544122	G	A	16	GENIC	homozygous	111524922
17	10544550	10544551	T	C	17	GENIC	homozygous	110954334
17	10545547	10545548	G	A	28	GENIC	homozygous	111524924
17	10545688	10545689	G	A	22	GENIC	homozygous	111524926
17	10545861	10545862	C	T	14	GENIC	homozygous	110954338
17	10546148	10546149	C	T	20	GENIC	homozygous	111524928
17	10546256	10546257	T	C	26	GENIC	homozygous	111637362
17	10546697	10546698	A	G	23	GENIC	homozygous	111524930
17	10546749	10546750	G	A	28	GENIC	homozygous	111524932
17	10546825	10546826	A	G	30	GENIC	homozygous	110954340
17	10546960	10546961	T	C	22	GENIC	homozygous	110954342
17	10547249	10547250	A	G	27	GENIC	possibly homozygous	111524934
17	10547571	10547572	C	T	25	GENIC	homozygous	111524936
17	10547720	10547721	C	T	27	GENIC	homozygous	111524938
17	10547856	10547857	A	C	26	GENIC	homozygous	111524940
17	10548488	10548489	G	A	27	GENIC	homozygous	111524942
17	10548665	10548666	C	T	28	GENIC	homozygous	111524944
17	10548721	10548722	C	T	24	GENIC	homozygous	111524946
17	10548996	10548997	A	G	15	GENIC	homozygous	111524948
17	10549194	10549195	G	A	26	GENIC	homozygous	111524950
17	10549728	10549729	G	T	14	GENIC	homozygous	111524952
17	10551170	10551171	G	A	29	GENIC	homozygous	111524954
17	10552353	10552354	T	C	22	GENIC	homozygous	111524956
17	10553201	10553202	C	T	18	GENIC	homozygous	111524958
17	10554013	10554014	A	G	32	GENIC	homozygous	111524960