chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	44968927	44968928	A	G	11	GENIC	homozygous	110692997
2	44968936	44968937	T	C	12	GENIC	homozygous	110930229
2	44968937	44968938	G	C	12	GENIC	homozygous	110930230
2	44968939	44968940	C	T	11	GENIC	homozygous	110930231
2	44969058	44969059	G	A	16	GENIC	homozygous	110692999
2	44969082	44969083	A	C	16	GENIC	homozygous	110508379
2	44969170	44969171	G	C	18	GENIC	homozygous	110693001
2	44969457	44969458	G	A	23	GENIC	homozygous	110693003
2	44972666	44972667	T	C	15	GENIC	homozygous	120167404
2	44972834	44972835	C	A	17	GENIC	homozygous	110508386
2	44973278	44973279	C	A	11	GENIC	homozygous	110508387
2	44973901	44973902	C	T	10	GENIC	homozygous	110508389
2	44974051	44974052	C	T	18	GENIC	homozygous	110508390
2	44974458	44974459	A	G	17	GENIC	homozygous	110508391
2	44974473	44974474	A	G	17	GENIC	homozygous	110508392
2	44970583	44970583		CAAGCAAGCAAG	6	GENIC	homozygous	131599791
2	44969206	44969206		GATT	14	GENIC	homozygous	130862144
2	44971349	44971350	A		8	GENIC	homozygous	130862148
2	44976090	44976096	GTGTGT		15	GENIC	homozygous	131599792
2	44977179	44977180	C	T	16	GENIC	homozygous	120189584
2	44979120	44979121	T	C	9	GENIC	homozygous	131608639
2	44979738	44979739	A	G	17	GENIC	heterozygous	109725789
2	44979737	44979738	A	G	17	GENIC	heterozygous	109725787
2	44979768	44979769	G	A	17	GENIC	heterozygous	109725791
2	44980105	44980106	A		8	GENIC	possibly homozygous	131599793
2	44980715	44980716	A	G	11	GENIC	homozygous	120167405