chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13128868	13128869	T	G	28	GENIC	homozygous	116735647
10	13129167	13129168	A	G	40	GENIC	homozygous	116735648
10	13129349	13129350	T	A	27	GENIC	homozygous	116735649
10	13130091	13130092	T	A	21	GENIC	homozygous	117150686
10	13130159	13130160	C	G	22	GENIC	homozygous	118030020
10	13130400	13130401	G	A	21	GENIC	homozygous	118079500
10	13130410	13130411	T	C	16	GENIC	homozygous	117215846
10	13130555	13130556	G	A	11	GENIC	homozygous	118079501
10	13130565	13130566	T	C	13	GENIC	homozygous	118030022
10	13131881	13131882	A	G	33	GENIC	possibly homozygous	116735650
10	13132115	13132116	T	A	33	GENIC	homozygous	116735651
10	13132247	13132248	G	A	40	GENIC	homozygous	116735652
10	13132739	13132740	A	G	34	GENIC	homozygous	116735653
10	13132962	13132963	A	C	54	GENIC	heterozygous	118030026
10	13132979	13132980	G	A	60	GENIC	heterozygous	118030028
10	13133216	13133217	T	C	38	GENIC	homozygous	116735654
10	13133802	13133803	A	G	14	GENIC	homozygous	116735655
10	13134137	13134138	G	T	54	GENIC	possibly homozygous	117074870
10	13135135	13135136	T	A	40	GENIC	homozygous	116859325
10	13135290	13135291	C	T	40	GENIC	homozygous	116735656
10	13135543	13135544	C	T	39	GENIC	homozygous	116735657
10	13135579	13135580	A	G	36	GENIC	homozygous	116735658
10	13135596	13135597	C	T	43	GENIC	homozygous	116735659
10	13143838	13143839	A	C	30	GENIC	homozygous	116735660
10	13146777	13146778	A	C	43	GENIC	homozygous	116735661
10	13147436	13147437	C	T	46	GENIC	homozygous	116735662
10	13148885	13148886	T	C	36	GENIC	homozygous	116735663
10	13149274	13149275	T	A	33	GENIC	homozygous	116735664
10	13149833	13149834	C	T	29	GENIC	homozygous	117120330
10	13149856	13149857	A	T	32	GENIC	heterozygous	116735665
10	13152029	13152030	T	C	61	GENIC	possibly homozygous	116735666
10	13154798	13154799	A	G	39	GENIC	homozygous	116735667
10	13160771	13160772	C	T	14	GENIC	homozygous	116735668
10	13162098	13162099	A	G	34	GENIC	homozygous	116735669
10	13141834	13141835	A	C	26	GENIC	homozygous	117982119