chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	71789744	71789745	T	C	34	GENIC	homozygous	111855468
16	71790009	71790010	A	C	26	GENIC	homozygous	119127793
16	71790041	71790042	A	C	20	GENIC	homozygous	119127795
16	71790953	71790954	C	T	43	GENIC	homozygous	112026989
16	71794669	71794670	G	A	39	GENIC	homozygous	111855470
16	71795325	71795326	C	T	36	GENIC	homozygous	112026991
16	71795474	71795475	G	A	44	GENIC	possibly homozygous	112132416
16	71795480	71795481	T	C	13	GENIC	heterozygous	119172735
16	71795520	71795521	G	A	39	GENIC	possibly homozygous	119210628
16	71795993	71795994	A	G	30	GENIC	homozygous	111855471
16	71797621	71797622	A	G	42	GENIC	homozygous	111855480
16	71798582	71798583	G	A	30	GENIC	homozygous	112026993
16	71799059	71799060	T	A	36	GENIC	heterozygous	119172739
16	71799088	71799089	C	T	36	GENIC	heterozygous	112077243
16	71799676	71799677	A	G	31	GENIC	homozygous	112132418
16	71800547	71800548	C	T	41	GENIC	homozygous	112026995
16	71801879	71801880	G	A	30	GENIC	homozygous	112026997
16	71802718	71802719	G	A	26	GENIC	homozygous	111855530