chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	210900633	210900634	A	C	34	INTERGENIC	homozygous	59373989
2	210900654	210900655	C	G	34	INTERGENIC	homozygous	59373991
2	210900662	210900663	C	A	29	INTERGENIC	homozygous	59373993
2	210900712	210900713	T	C	26	INTERGENIC	homozygous	59373995
2	210900719	210900720	T	G	28	INTERGENIC	homozygous	59373997
2	210900723	210900724	C	A	31	INTERGENIC	homozygous	59373999
2	210900728	210900729	C	T	35	INTERGENIC	homozygous	59374001
2	210900729	210900730	C	T	36	INTERGENIC	homozygous	59374003
2	210900731	210900732	C	G	36	INTERGENIC	homozygous	59374005
2	210900974	210900975	G	-	32	INTERGENIC	homozygous	59374007
2	210917445	210917446	A	AATTTATTTATTT	1	INTERGENIC	homozygous	60515917
2	210923489	210923490	C	-	24	INTERGENIC	homozygous	59374097
2	210926881	210926882	T	TTGTGTG	13	INTERGENIC	heterozygous	59374123
2	210926881	210926882	T	TTGTG	13	INTERGENIC	heterozygous	59374125
2	210926881	210926882	T	TTG	13	INTERGENIC	heterozygous	60548546
2	210929425	210929427	TG	--	7	INTERGENIC	possibly homozygous	60586248
2	210931535	210931536	T	TAACA	22	INTERGENIC	homozygous	61263502
2	210934208	210934210	CT	--	3	INTERGENIC	homozygous	62203164