chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41214988	41214989	G	A	8	GENIC	homozygous	115426832
12	41215326	41215327	G	A	21	GENIC	homozygous	115329636
12	41215494	41215495	T	A	13	GENIC	homozygous	115329638
12	41215509	41215510	G	A	13	GENIC	homozygous	115329640
12	41215661	41215662	C	T	22	GENIC	homozygous	115329642
12	41216005	41216006	C	A	16	GENIC	homozygous	115329644
12	41216209	41216210	A	G	17	GENIC	homozygous	115329646
12	41216213	41216214	T	C	17	GENIC	homozygous	115329648
12	41216475	41216476	A	G	13	GENIC	homozygous	115329650
12	41216740	41216741	A	G	18	GENIC	homozygous	115329652
12	41216783	41216784	C	T	26	GENIC	homozygous	115329654
12	41217146	41217147	T	G	19	GENIC	homozygous	115329656
12	41218122	41218123	A	G	15	GENIC	homozygous	115329664
12	41218501	41218502	G	A	16	GENIC	homozygous	115329666
12	41218578	41218579	A	T	16	GENIC	homozygous	115329668
12	41220128	41220129	G	A	4	GENIC	homozygous	115668498
12	41218934	41218935	C	T	7	GENIC	homozygous	115668492
12	41220126	41220127	C	T	3	GENIC	homozygous	115668494
12	41220127	41220128	A	G	3	GENIC	homozygous	115668496
12	41220561	41220562	C	G	26	GENIC	homozygous	115426834
12	41220938	41220939	C	T	21	GENIC	homozygous	115329670
12	41221566	41221567	T	C	16	GENIC	homozygous	115329674
12	41221843	41221844	A	G	22	GENIC	homozygous	115329676
12	41222056	41222057	C	T	9	GENIC	homozygous	115329678
12	41223704	41223705	A	G	36	GENIC	homozygous	115329694