chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	104190134	104190135	T	C	28	GENIC	homozygous	116619786
8	104192332	104192333	A	G	32	GENIC	homozygous	116619788
8	104193159	104193160	C	T	28	GENIC	homozygous	116619790
8	104193476	104193477	A	C	36	GENIC	homozygous	116619792
8	104193690	104193691	A	G	36	GENIC	homozygous	116619794
8	104193863	104193864	A	G	35	GENIC	homozygous	116619796
8	104193883	104193884	C	G	33	GENIC	homozygous	116619798
8	104194032	104194033	T	C	28	GENIC	homozygous	116619800
8	104194351	104194352	A	G	31	GENIC	homozygous	116619802
8	104195255	104195256	C	A	18	GENIC	homozygous	116619804
8	104196866	104196867	G	C	41	GENIC	homozygous	116619806
8	104197708	104197709	C	A	36	GENIC	homozygous	116619808
8	104197885	104197886	T	C	26	GENIC	homozygous	116619810
8	104199271	104199272	C	T	30	GENIC	homozygous	116619822
8	104200834	104200835	T	C	28	GENIC	homozygous	116619826
8	104203283	104203284	C	T	20	GENIC	homozygous	116619828
8	104206695	104206696	G	A	30	GENIC	homozygous	116619830
8	104206976	104206977	A	T	27	GENIC	homozygous	117911978
8	104208647	104208648	A	T	30	GENIC	homozygous	116619832
8	104209513	104209514	T	A	22	GENIC	homozygous	116619836
8	104209715	104209716	G	A	28	GENIC	homozygous	116619838
8	104209812	104209813	C	T	28	GENIC	homozygous	116619840
8	104210371	104210372	G	A	38	GENIC	homozygous	116619842
8	104212906	104212907	T	C	36	GENIC	homozygous	116619844
8	104213074	104213075	G	A	25	GENIC	homozygous	116619846
8	104213538	104213539	T	C	19	GENIC	homozygous	116619848
8	104213864	104213865	A	G	30	GENIC	homozygous	116619850
8	104214072	104214073	A	G	28	GENIC	homozygous	116619852
8	104214092	104214093	T	C	26	GENIC	homozygous	116619854