chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	214786007	214786008	C	T	17	GENIC	heterozygous	62587682
1	214788360	214788361	T	TC	5	GENIC	heterozygous	62587683
1	214791998	214791999	A	G	12	GENIC	homozygous	61965211
1	214795881	214795882	G	A	32	GENIC	possibly homozygous	62587684
1	214796398	214796399	T	C	7	GENIC	homozygous	61965234
1	214796688	214796689	A	G	14	GENIC	homozygous	62035812
1	214797939	214797940	T	C	13	GENIC	heterozygous	62587685
1	214798169	214798170	C	T	7	GENIC	possibly homozygous	61965245
1	214803328	214803329	A	G	12	GENIC	possibly homozygous	61965248
1	214803544	214803545	G	GCA	7	GENIC	homozygous	62099629
1	214804182	214804183	A	T	14	GENIC	homozygous	61965252
1	214804869	214804870	A	G	2	GENIC	homozygous	61965255
1	214806082	214806083	A	T	14	GENIC	possibly homozygous	62587687
1	214807537	214807538	T	C	21	GENIC	homozygous	61965260
1	214808322	214808323	C	T	6	GENIC	heterozygous	62587689
1	214812560	214812561	T	TG	5	GENIC	heterozygous	62587690
1	214812560	214812561	T	TGG	5	GENIC	heterozygous	62587691
1	214812971	214812972	A	G	13	GENIC	homozygous	62587692
1	214813634	214813635	C	T	16	GENIC	homozygous	62485474