chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44046295	44046296	C	G	26	GENIC	homozygous	115336630
12	44046303	44046304	T	C	27	GENIC	homozygous	115336632
12	44056243	44056244	A	G	38	GENIC	homozygous	115390240
12	44057170	44057171	G	A	26	GENIC	homozygous	115390242
12	44054993	44054994	T	A	43	GENIC	homozygous	115390236
12	44055732	44055733	A	G	33	GENIC	homozygous	115390238
12	44058511	44058512	G	A	35	GENIC	homozygous	115390244
12	44058599	44058600	A	C	29	GENIC	homozygous	115390246
12	44059426	44059427	G	A	42	GENIC	homozygous	115390248
12	44061679	44061680	G	A	27	GENIC	possibly homozygous	115390250
12	44061917	44061918	T	C	39	GENIC	possibly homozygous	118305875
12	44062154	44062155	T	A	24	GENIC	possibly homozygous	115390252
12	44062849	44062850	C	T	34	GENIC	homozygous	115390254
12	44059800	44059801	A	G	15	GENIC	homozygous	115430124
12	44064237	44064238	G	A	34	GENIC	homozygous	115430126
12	44072579	44072580	C	T	28	GENIC	homozygous	115390256
12	44073578	44073579	A	G	35	GENIC	homozygous	115336638
12	44073769	44073770	T	C	15	GENIC	homozygous	115390258
12	44074709	44074710	A	G	32	GENIC	homozygous	115390260
12	44077805	44077806	C	T	28	GENIC	homozygous	115390262
12	44078677	44078678	A	G	38	GENIC	possibly homozygous	115390264
12	44081007	44081008	C	A	20	GENIC	possibly homozygous	118271721
12	44076688	44076689	A	G	30	GENIC	possibly homozygous	118271720
12	44081455	44081456	T	C	36	GENIC	homozygous	115390266
12	44083924	44083925	A	G	32	GENIC	homozygous	115390268
12	44086202	44086203	C	A	33	GENIC	homozygous	115390270
12	44088841	44088842	A	G	36	GENIC	homozygous	115390272
12	44128942	44128943	C	T	26	GENIC	homozygous	115390274