chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	75150147	75150148	C	G	53	GENIC	homozygous	116638399
10	75151175	75151176	T	G	38	GENIC	possibly homozygous	116638401
10	75151986	75151987	C	A	43	GENIC	heterozygous	118124512
10	75152423	75152424	C	T	40	GENIC	homozygous	116638403
10	75152703	75152704	C	G	45	GENIC	homozygous	116638405
10	75153566	75153567	A	G	46	GENIC	homozygous	116638407
10	75154306	75154307	G	A	53	GENIC	homozygous	116638409
10	75155195	75155196	G	A	59	GENIC	homozygous	116638411
10	75155371	75155372	C	G	66	GENIC	possibly homozygous	116638413
10	75155429	75155430	T	C	57	GENIC	homozygous	116638414
10	75158487	75158488	G	A	61	GENIC	homozygous	116638416
10	75158625	75158626	G	A	57	GENIC	homozygous	117065587
10	75158663	75158664	C	T	58	GENIC	homozygous	117065589
10	75158916	75158917	C	G	38	GENIC	possibly homozygous	116638418
10	75158994	75158995	T	C	52	GENIC	homozygous	116638420
10	75159674	75159675	T	C	44	GENIC	homozygous	116638422
10	75160468	75160469	A	G	49	GENIC	homozygous	116638424