chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	87211650	87211651	G	T	14	GENIC	homozygous	136206522
2	87213425	87213425		A	30	GENIC	homozygous	135925303
2	87214813	87214813		TATT	24	GENIC	possibly homozygous	135925304
2	87216092	87216093	A		23	GENIC	homozygous	135925305
2	87216564	87216565	C	T	23	GENIC	homozygous	136206523
2	87217301	87217302	A	G	28	GENIC	homozygous	136206524
2	87217350	87217351	A	T	26	GENIC	homozygous	136206525
2	87217617	87217618	C	T	21	GENIC	possibly homozygous	148448997
2	87218278	87218279	C		11	GENIC	homozygous	135925306
2	87220912	87220913	T	C	24	GENIC	homozygous	136206526
2	87221053	87221054	T	C	22	GENIC	homozygous	136206527
2	87222058	87222059	T	C	18	GENIC	homozygous	136206528
2	87222320	87222321	C	T	38	GENIC	homozygous	136206529
2	87223292	87223293	A	G	20	GENIC	homozygous	136206530
2	87223860	87223861	C	A	30	GENIC	homozygous	136206531
2	87224034	87224035	C	T	26	GENIC	homozygous	136206532
2	87225128	87225129	T	C	20	GENIC	homozygous	136206533
2	87226587	87226588	C	G	11	GENIC	homozygous	136206536
2	87225343	87225344	A	G	22	GENIC	homozygous	136206534
2	87225712	87225713	G	T	22	GENIC	homozygous	136206535
2	87226821	87226821		A	11	GENIC	homozygous	135925307
2	87227303	87227304	C	T	24	GENIC	homozygous	136206537
2	87227744	87227745	C	T	26	GENIC	homozygous	136206538
2	87228895	87228896	A	G	18	GENIC	homozygous	136206539
2	87230129	87230130	T	C	24	GENIC	homozygous	136206540