chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	44968927	44968928	A	G	10	GENIC	homozygous	110692997
2	44968936	44968937	T	C	11	GENIC	homozygous	110930229
2	44968937	44968938	G	C	10	GENIC	homozygous	110930230
2	44968939	44968940	C	T	9	GENIC	homozygous	110930231
2	44969058	44969059	G	A	10	GENIC	homozygous	110692999
2	44969082	44969083	A	C	17	GENIC	homozygous	110508379
2	44969170	44969171	G	C	5	GENIC	homozygous	110693001
2	44969457	44969458	G	A	20	GENIC	homozygous	110693003
2	44970586	44970587	T	G	16	GENIC	heterozygous	110508385
2	44972834	44972835	C	A	12	GENIC	homozygous	110508386
2	44973566	44973567	C	A	11	GENIC	homozygous	110508388
2	44973901	44973902	C	T	17	GENIC	homozygous	110508389
2	44972666	44972667	T	C	11	GENIC	homozygous	120167404
2	44974051	44974052	C	T	15	GENIC	homozygous	110508390
2	44974458	44974459	A	G	20	GENIC	homozygous	110508391
2	44974473	44974474	A	G	13	GENIC	homozygous	110508392
2	44977179	44977180	C	T	17	GENIC	homozygous	120189584
2	44976087	44976088	C	G	5	GENIC	heterozygous	125685039
2	44980715	44980716	A	G	18	GENIC	homozygous	120167405