chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	45886636	45886637	T	A	12	GENIC	homozygous	50339312
12	45887375	45887376	A	G	13	GENIC	possibly homozygous	50339314
12	45887886	45887887	A	G	3	GENIC	heterozygous	50339316
12	45888813	45888814	G	A	15	GENIC	heterozygous	50339318
12	45889840	45889841	A	-	14	GENIC	homozygous	50339320
12	45890154	45890155	G	A	10	GENIC	possibly homozygous	50339322
12	45890242	45890243	A	C	14	GENIC	heterozygous	50339324
12	45891069	45891070	G	A	20	GENIC	possibly homozygous	50339326
12	45891443	45891444	A	G	9	GENIC	possibly homozygous	50339328
12	45891707	45891708	T	-	7	GENIC	heterozygous	50545546
12	45893322	45893323	G	A	8	GENIC	heterozygous	50339330
12	45893797	45893798	T	A	23	GENIC	possibly homozygous	50339334
12	45894492	45894493	C	T	18	GENIC	possibly homozygous	50339336
12	45895880	45895881	G	A	23	GENIC	homozygous	50339338
12	45900791	45900792	T	TATA	10	GENIC	homozygous	50339344
12	45904222	45904223	C	T	17	GENIC	possibly homozygous	50339346
12	45905221	45905222	A	G	15	GENIC	possibly homozygous	50217647
12	45905402	45905403	T	C	10	GENIC	heterozygous	50386725
12	45905853	45905854	C	-	10	GENIC	possibly homozygous	50217648
12	45906352	45906353	A	G	18	GENIC	possibly homozygous	50339350
12	45909448	45909449	C	T	2	GENIC	homozygous	50339352
12	45910320	45910321	A	G	13	GENIC	possibly homozygous	50339354
12	45913098	45913099	T	C	14	GENIC	homozygous	50339356
12	45915567	45915568	A	G	23	GENIC	possibly homozygous	50339358
12	45917845	45917846	C	A	14	GENIC	homozygous	50339360
12	45920484	45920485	A	G	18	GENIC	homozygous	50339364
12	45959392	45959393	G	A	9	GENIC	heterozygous	50592563
12	45960585	45960586	C	T	5	GENIC	homozygous	50339374