chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	191319151	191319152	C	T	31	GENIC	homozygous	136418118
2	191319784	191319785	T	A	15	GENIC	homozygous	136418119
2	191320797	191320798	C	T	14	GENIC	homozygous	136418120
2	191322261	191322262	G	A	24	GENIC	homozygous	136418121
2	191322665	191322666	C	T	24	GENIC	homozygous	136418122
2	191325546	191325547	G	A	29	GENIC	homozygous	136418123
2	191325777	191325778	C	T	22	GENIC	homozygous	136418124
2	191325939	191325940	T	C	24	GENIC	heterozygous	403034032
2	191325939	191325941	TG		24	GENIC	homozygous	135968857
2	191322348	191322348		T	23	GENIC	possibly homozygous	135968854
2	191325803	191325831	TGCATCACCAGTGCTCGTATTTAAAGTG		23	GENIC	homozygous	135968855
2	191325936	191325936		TT	24	GENIC	homozygous	135968856
2	191325936	191325937	C	A	24	GENIC	homozygous	403034029
2	191325936	191325937	C	T	24	GENIC	heterozygous	403034030
2	191325939	191325940	T		24	GENIC	homozygous	403034031
2	191325949	191325950	G	A	24	GENIC	homozygous	136418125
2	191325996	191325997	T	A	18	GENIC	homozygous	136418126
2	191325997	191325998	C	T	18	GENIC	homozygous	136418127
2	191326907	191326908	G	T	20	GENIC	homozygous	136418128
2	191327061	191327062	G	A	12	GENIC	homozygous	136418129
2	191328712	191328713	T	C	30	GENIC	homozygous	136418130
2	191329707	191329708	A	G	15	GENIC	homozygous	136418131