chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	38058827	38058828	G	A	16	GENIC	homozygous	115322389
12	38058845	38058846	G	A	17	GENIC	homozygous	115322391
12	38058860	38058861	G	A	18	GENIC	homozygous	115322393
12	38058938	38058939	G	C	18	GENIC	homozygous	115322395
12	38059177	38059178	C	T	19	GENIC	homozygous	115322397
12	38059444	38059445	G	A	17	GENIC	homozygous	115322399
12	38060427	38060428	G	A	21	GENIC	homozygous	115322401
12	38061999	38062000	G	A	28	GENIC	homozygous	115322403
12	38062259	38062260	G	A	20	GENIC	homozygous	115322405
12	38062639	38062640	G	A	29	GENIC	homozygous	115322407
12	38066268	38066269	G	A	28	GENIC	homozygous	115322409
12	38069053	38069054	G	A	16	GENIC	homozygous	115322413
12	38071207	38071208	G	A	22	GENIC	homozygous	115322415
12	38073496	38073497	T	C	23	GENIC	homozygous	115322417
12	38076400	38076401	T	G	19	GENIC	homozygous	115322419
12	38077513	38077514	A	G	14	GENIC	homozygous	115322421
12	38081449	38081450	T	A	23	GENIC	homozygous	115322423
12	38083069	38083070	A	G	16	GENIC	homozygous	115381746
12	38083077	38083078	G	A	19	GENIC	homozygous	115381748
12	38083634	38083635	C	G	28	GENIC	homozygous	115322425
12	38083764	38083765	C	A	46	GENIC	homozygous	115322427
12	38083795	38083796	G	A	49	GENIC	homozygous	115322429
12	38084683	38084684	A	G	32	GENIC	homozygous	115322431
12	38087038	38087039	C	T	23	GENIC	homozygous	115322433
12	38092745	38092746	G	A	32	GENIC	homozygous	115322435