chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	62400273	62400274	G	T	38	GENIC	homozygous	113235799
4	62401282	62401283	A	G	30	GENIC	homozygous	112672438
4	62402522	62402523	A	T	28	GENIC	homozygous	112672440
4	62403572	62403573	A	G	22	GENIC	homozygous	112672442
4	62408260	62408261	A	T	31	GENIC	homozygous	113235800
4	62410011	62410012	C	T	33	GENIC	homozygous	113235801
4	62413739	62413740	A	C	21	GENIC	homozygous	112672449
4	62416669	62416670	C	T	5	GENIC	homozygous	113235802
4	62417157	62417158	G	T	28	GENIC	homozygous	112672451
4	62417203	62417204	G	A	24	GENIC	homozygous	113235803
4	62417264	62417265	C	T	20	GENIC	homozygous	113235804
4	62431280	62431281	T	C	23	GENIC	homozygous	112672471
4	62432132	62432133	G	T	27	GENIC	homozygous	113235807
4	62432512	62432513	T	C	30	GENIC	homozygous	113235808
4	62433386	62433387	A	G	27	GENIC	homozygous	113235809
4	62433392	62433393	G	A	28	GENIC	homozygous	113235810
4	62435309	62435310	T	C	9	GENIC	homozygous	112672473
4	62435416	62435417	C	T	28	GENIC	homozygous	112672475
4	62435754	62435755	A	T	18	GENIC	homozygous	113235811
4	62436820	62436821	G	A	23	GENIC	homozygous	113235812
4	62438393	62438394	C	G	25	GENIC	homozygous	113235813