chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	50362586	50362587	T	C	12	GENIC	possibly homozygous	113792260
5	50362620	50362621	C	T	15	GENIC	homozygous	119248988
5	50362700	50362701	T	G	35	GENIC	possibly homozygous	113792261
5	50363116	50363117	C	A	23	GENIC	homozygous	113792262
5	50374553	50374554	T	C	11	GENIC	heterozygous	113792265
5	50382650	50382651	A	T	18	GENIC	possibly homozygous	113792266
5	50382674	50382675	C	T	16	GENIC	homozygous	113792267
5	50383614	50383615	A	G	28	GENIC	possibly homozygous	113792271
5	50389786	50389787	A	G	20	GENIC	possibly homozygous	113792274
5	50390002	50390003	C	G	35	GENIC	possibly homozygous	113792275
5	50390560	50390561	A	T	23	GENIC	possibly homozygous	113792276