chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	3956946	3956947	C	G	9	GENIC	homozygous	112995991
4	3995258	3995259	C	G	13	GENIC	homozygous	112468265
4	3962692	3962693	T	G	7	GENIC	homozygous	112468257
4	3979618	3979619	G	C	26	GENIC	homozygous	112468259
4	3990806	3990807	T	C	27	GENIC	homozygous	112468261
4	3994986	3994987	C	T	10	GENIC	homozygous	112468263
4	3972385	3972386	G	A	29	GENIC	possibly homozygous	113428904
4	3978798	3978799	A	G	32	GENIC	homozygous	113428906
4	3995260	3995261	C	A	13	GENIC	homozygous	112468267
4	3995262	3995263	G	T	13	GENIC	homozygous	112468269
4	3995305	3995306	C	T	10	GENIC	homozygous	112468271
4	3995391	3995392	G	T	13	GENIC	homozygous	112468273
4	3996848	3996849	C	G	23	GENIC	heterozygous	113428908
4	4006400	4006401	A	C	36	GENIC	heterozygous	112468275
4	4006408	4006409	A	G	36	GENIC	heterozygous	112468277
4	4006423	4006424	T	G	37	GENIC	heterozygous	112468279