chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	189841521	189841522	T	C	28	GENIC	homozygous	110172114
2	189841629	189841630	T	C	14	GENIC	homozygous	110172115
2	189841989	189841990	G	A	15	GENIC	possibly homozygous	110172117
2	189842247	189842248	A	G	15	GENIC	possibly homozygous	110906312
2	189844262	189844263	G	A	16	GENIC	homozygous	110805118
2	189845059	189845060	C	T	26	GENIC	homozygous	110805119
2	189845692	189845693	G	A	29	GENIC	heterozygous	110805120
2	189846796	189846797	G	A	24	GENIC	homozygous	110805121
2	189847825	189847826	C	T	15	GENIC	homozygous	110805122
2	189848559	189848560	A	G	27	GENIC	homozygous	110172119
2	189848577	189848578	C	A	27	GENIC	homozygous	110805123
2	189849730	189849731	A	G	34	GENIC	homozygous	110805124
2	189850288	189850289	C	T	12	GENIC	homozygous	110805125
2	189850481	189850482	G	A	30	GENIC	homozygous	110805126
2	189850600	189850601	G	C	15	GENIC	possibly homozygous	110805127
2	189851040	189851041	C	A	34	GENIC	homozygous	110805128
2	189851056	189851057	G	A	35	GENIC	homozygous	110805129
2	189851852	189851853	T	C	23	GENIC	homozygous	110805130
2	189852164	189852165	G	T	23	GENIC	homozygous	110805131
2	189852386	189852387	G	A	24	GENIC	homozygous	110805132
2	189854130	189854131	C	T	24	GENIC	homozygous	110805133
2	189854195	189854196	C	A	27	GENIC	heterozygous	110805134
2	189854287	189854288	C	G	27	GENIC	homozygous	110172123