chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31074708	31074709	T	G	9	GENIC	homozygous	116545552
10	31076758	31076759	G	A	31	GENIC	homozygous	116545554
10	31078017	31078018	G	C	23	GENIC	homozygous	116545556
10	31080259	31080260	G	A	27	GENIC	homozygous	116545558
10	31081234	31081235	G	T	31	GENIC	homozygous	116545560
10	31081881	31081882	A	C	22	GENIC	homozygous	116545562
10	31082636	31082637	T	G	32	GENIC	homozygous	116545564
10	31084443	31084444	A	G	33	GENIC	homozygous	116545566
10	31085223	31085224	G	T	25	GENIC	homozygous	117250823
10	31085406	31085407	C	T	41	GENIC	homozygous	116545568
10	31085625	31085626	C	T	39	GENIC	homozygous	116545570
10	31085652	31085653	G	A	41	GENIC	homozygous	116545572
10	31085711	31085712	C	T	29	GENIC	homozygous	116545574
10	31085734	31085735	C	T	34	GENIC	homozygous	116545576
10	31085736	31085737	C	T	34	GENIC	homozygous	116545578
10	31085749	31085750	C	T	33	GENIC	homozygous	117250825
10	31085753	31085754	C	T	34	GENIC	homozygous	117250827
10	31085785	31085786	C	T	39	GENIC	homozygous	117250829
10	31085795	31085796	C	T	38	GENIC	homozygous	116752435