chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44008955	44008956	T	A	19	GENIC	homozygous	115479374
12	44010252	44010253	A	T	30	GENIC	homozygous	115479376
12	44010405	44010406	G	A	37	GENIC	homozygous	115479378
12	44011676	44011677	T	C	29	GENIC	homozygous	115336608
12	44012288	44012289	A	G	17	GENIC	homozygous	115336610
12	44012467	44012468	T	G	9	GENIC	homozygous	115479380
12	44015731	44015732	G	A	33	GENIC	homozygous	115479382
12	44016186	44016187	A	T	33	GENIC	homozygous	115390200
12	44016227	44016228	G	A	21	GENIC	homozygous	115479384
12	44016306	44016307	A	G	31	GENIC	homozygous	115479386
12	44016887	44016888	A	G	33	GENIC	homozygous	115390202
12	44017080	44017081	C	A	35	GENIC	homozygous	115390204
12	44017186	44017187	A	G	32	GENIC	homozygous	115479388
12	44017455	44017456	A	T	23	GENIC	homozygous	115479390
12	44019153	44019154	C	T	32	GENIC	homozygous	115479392
12	44019879	44019880	C	T	38	GENIC	homozygous	115479394
12	44019964	44019965	T	A	22	GENIC	homozygous	115479396
12	44020780	44020781	T	C	20	GENIC	homozygous	115479398
12	44020947	44020948	A	G	31	GENIC	homozygous	115390208
12	44021630	44021631	G	A	30	GENIC	homozygous	115390210
12	44022700	44022701	G	A	40	GENIC	homozygous	115479400
12	44029184	44029185	T	C	4	GENIC	homozygous	115336614