chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	43634278	43634279	A	G	8	GENIC	possibly homozygous	115335411
12	43634391	43634392	G	A	8	GENIC	homozygous	115335413
12	43634407	43634408	A	T	10	GENIC	homozygous	115389569
12	43634573	43634574	G	A	11	GENIC	possibly homozygous	115335416
12	43634994	43634995	T	C	7	GENIC	homozygous	115335418
12	43635251	43635252	T	C	5	GENIC	homozygous	115335420
12	43635313	43635314	T	C	5	GENIC	homozygous	115335422
12	43635436	43635437	G	T	8	GENIC	homozygous	115335424
12	43636469	43636470	A	T	8	GENIC	homozygous	115335428
12	43637077	43637078	A	T	10	GENIC	homozygous	115389571
12	43637452	43637453	C	T	8	GENIC	homozygous	115335430
12	43638607	43638608	T	A	4	GENIC	homozygous	115335432
12	43639170	43639171	G	A	10	GENIC	homozygous	115335434
12	43639462	43639463	G	A	10	GENIC	homozygous	115335436
12	43640223	43640224	A	G	7	GENIC	homozygous	115335440
12	43640485	43640486	T	C	16	GENIC	homozygous	115335444
12	43640672	43640673	T	C	11	GENIC	homozygous	115335446
12	43640780	43640781	T	C	8	GENIC	homozygous	115335450