chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	104934539	104934540	T		17	GENIC	homozygous	127660577
2	104934554	104934554		C	17	GENIC	homozygous	127660578
2	104934616	104934616		G	16	GENIC	homozygous	127660579
2	104934625	104934626	G		17	GENIC	homozygous	127660580
2	104934652	104934653	T		16	GENIC	homozygous	127660581
2	104934724	104934725	A		17	GENIC	homozygous	127660582
2	104934741	104934741		C	14	GENIC	homozygous	127660583
2	104934744	104934745	T		14	GENIC	homozygous	127660584
2	104937912	104937913	C	A	29	GENIC	homozygous	109961631
2	104937951	104937952	C	G	24	GENIC	homozygous	109961633
2	104937968	104937969	C		25	GENIC	homozygous	127660595
2	104937984	104937985	C	G	27	GENIC	homozygous	109961635
2	104937995	104937996	C	A	18	GENIC	homozygous	109961637
2	104937997	104937998	C	G	18	GENIC	homozygous	109961639
2	104938010	104938011	T	G	19	GENIC	homozygous	110580165
2	104938012	104938013	C	T	17	GENIC	homozygous	109961641