chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90211441	90211442	G	A	12	GENIC	homozygous	68165194
10	90212356	90212357	G	A	15	GENIC	homozygous	68165197
10	90214177	90214178	C	T	38	GENIC	homozygous	68455203
10	90214912	90214913	T	A	20	GENIC	homozygous	68165200
10	90215154	90215155	G	A	29	GENIC	homozygous	68165203
10	90216961	90216962	T	C	33	GENIC	homozygous	68165206
10	90219945	90219946	C	A	19	GENIC	homozygous	68165219
10	90219951	90219952	C	A	18	GENIC	possibly homozygous	68165222
10	90220311	90220312	G	A	17	GENIC	homozygous	68165225
10	90221554	90221555	A	C	26	GENIC	homozygous	68165228
10	90221782	90221783	A	G	14	GENIC	homozygous	68165231
10	90222434	90222435	T	C	30	GENIC	homozygous	68165234
10	90222723	90222724	C	T	24	GENIC	homozygous	68165237
10	90223023	90223024	A	G	23	GENIC	homozygous	68165240
10	90224161	90224162	C	T	18	GENIC	possibly homozygous	68165246
10	90224173	90224174	A	G	20	GENIC	homozygous	68165249
10	90226080	90226081	A	G	11	GENIC	homozygous	68165256
10	90226696	90226697	T	A	19	GENIC	homozygous	68455206
10	90227640	90227641	C	A	21	GENIC	homozygous	68455209
10	90233044	90233045	T	C	38	GENIC	homozygous	68165277
10	90219986	90219987	A	T	13	GENIC	heterozygous	82695808