chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13128868	13128869	T	G	34	GENIC	homozygous	116735647
10	13129167	13129168	A	G	21	GENIC	homozygous	116735648
10	13129349	13129350	T	A	28	GENIC	homozygous	116735649
10	13131400	13131401	G	A	25	GENIC	homozygous	116915000
10	13131881	13131882	A	G	21	GENIC	homozygous	116735650
10	13132247	13132248	G	A	23	GENIC	homozygous	116735652
10	13132739	13132740	A	G	19	GENIC	homozygous	116735653
10	13133216	13133217	T	C	17	GENIC	homozygous	116735654
10	13133802	13133803	A	G	10	GENIC	homozygous	116735655
10	13135135	13135136	T	A	10	GENIC	homozygous	116859325
10	13135290	13135291	C	T	25	GENIC	homozygous	116735656
10	13135543	13135544	C	T	31	GENIC	homozygous	116735657
10	13135579	13135580	A	G	35	GENIC	homozygous	116735658
10	13135596	13135597	C	T	39	GENIC	homozygous	116735659
10	13138285	13138286	C	G	25	GENIC	homozygous	116915002
10	13138821	13138822	C	T	24	GENIC	homozygous	116915004
10	13139029	13139030	A	G	22	GENIC	homozygous	116915006
10	13143838	13143839	A	C	17	GENIC	homozygous	116735660
10	13148885	13148886	T	C	15	GENIC	homozygous	116735663
10	13152029	13152030	T	C	17	GENIC	homozygous	116735666
10	13154798	13154799	A	G	38	GENIC	homozygous	116735667
10	13155752	13155753	G	C	21	GENIC	homozygous	116915008
10	13162098	13162099	A	G	32	GENIC	homozygous	116735669
10	13162816	13162817	G	A	28	GENIC	homozygous	116915010