chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	36101433	36101434	C	T	46	GENIC	possibly homozygous	147004556
12	36101536	36101537	C	T	61	GENIC	homozygous	147004557
12	36101704	36101705	A	G	50	GENIC	homozygous	147004558
12	36101740	36101741	T	A	48	GENIC	homozygous	139137401
12	36102984	36102985	C	T	38	GENIC	homozygous	147004559
12	36103100	36103101	A	C	46	GENIC	homozygous	147004560
12	36103889	36103890	G	A	56	GENIC	homozygous	147004561
12	36104788	36104789	G	T	24	GENIC	homozygous	147004562
12	36105209	36105210	T	C	37	GENIC	homozygous	139137403
12	36106543	36106544	A	C	49	GENIC	homozygous	139137405
12	36106591	36106592	C	T	44	GENIC	homozygous	147004563
12	36107032	36107033	C	T	55	GENIC	homozygous	139137406
12	36107851	36107852	A	G	68	GENIC	homozygous	147004564
12	36108889	36108890	T	C	63	GENIC	homozygous	139137408
12	36109099	36109100	A	G	46	GENIC	homozygous	147004565
12	36106055	36106055		C	34	GENIC	homozygous	139054091
12	36104882	36104882		T	14	GENIC	possibly homozygous	147000262