chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	211183887	211183888	G		56	GENIC	homozygous	131811628
2	211184219	211184220	C	T	48	GENIC	homozygous	111421139
2	211187709	211187736	CCGCCATGATGCTCTCTATACCAACAC		49	GENIC	homozygous	131811629
2	211188398	211188399	G	A	55	GENIC	homozygous	111421140
2	211189673	211189674	C	T	67	GENIC	homozygous	111421141
2	211191321	211191331	TCTTTTTTTC		31	GENIC	homozygous	131811630
2	211192860	211192861	A	T	54	GENIC	homozygous	111421142
2	211194047	211194048	T	C	68	GENIC	homozygous	110909350
2	211194388	211194389	C	T	74	GENIC	homozygous	110909352
2	211194767	211194768	G	A	66	GENIC	possibly homozygous	111421143
2	211195301	211195302	C	T	49	GENIC	homozygous	111421144
2	211196241	211196242	A	G	57	GENIC	homozygous	110224195
2	211197056	211197057	T	C	61	GENIC	homozygous	110224197
2	211198064	211198065	C		12	GENIC	possibly homozygous	127732932
2	211198162	211198163	G	A	33	GENIC	homozygous	111421145
2	211202253	211202253		AAAGACCCAGGA	54	GENIC	homozygous	127732933
2	211204666	211204667	T	C	55	GENIC	homozygous	111421149
2	211200108	211200109	T	C	60	GENIC	possibly homozygous	110224201
2	211200569	211200570	G	A	49	GENIC	possibly homozygous	111421146
2	211204501	211204502	G	A	59	GENIC	homozygous	111421148
2	211205658	211205659	G	A	57	GENIC	possibly homozygous	111421150
2	211206148	211206149	A	G	59	GENIC	homozygous	110224205