chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23545038	23545039	A	G	14	GENIC	homozygous	115284993
12	23547224	23547225	G	A	33	GENIC	homozygous	115446039
12	23548240	23548241	T	C	23	GENIC	homozygous	115285003
12	23549188	23549189	G	T	36	GENIC	homozygous	115285009
12	23549237	23549238	C	T	33	GENIC	homozygous	115368426
12	23549655	23549656	C	T	40	GENIC	possibly homozygous	115285011
12	23549710	23549711	A	G	39	GENIC	homozygous	115285013
12	23550107	23550108	T	C	21	GENIC	homozygous	115285017
12	23550166	23550167	C	T	30	GENIC	homozygous	115285019
12	23550376	23550377	C	T	23	GENIC	homozygous	115368428
12	23551525	23551526	C	T	20	GENIC	homozygous	115368430
12	23552336	23552337	T	C	17	GENIC	homozygous	115368432
12	23552544	23552545	T	C	25	GENIC	homozygous	115368434
12	23552618	23552619	A	G	12	GENIC	homozygous	115285029
12	23553440	23553441	C	T	12	GENIC	homozygous	115285031
12	23553910	23553911	G	A	15	GENIC	homozygous	115368436
12	23556166	23556167	C	T	24	GENIC	homozygous	115368438
12	23556684	23556685	G	A	23	GENIC	homozygous	115285041
12	23558051	23558052	A	C	29	GENIC	homozygous	115285049
12	23556747	23556748	T	C	11	GENIC	homozygous	115285043
12	23556790	23556791	A	C	13	GENIC	homozygous	115285045
12	23560275	23560276	A	G	17	GENIC	homozygous	115285063
12	23563278	23563279	G	A	13	GENIC	homozygous	115469720
12	23563386	23563387	T	C	20	GENIC	homozygous	115368440