chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	44968927	44968928	A	G	36	GENIC	homozygous	110692997
2	44968936	44968937	T	C	38	GENIC	homozygous	110930229
2	44968937	44968938	G	C	37	GENIC	homozygous	110930230
2	44968939	44968940	C	T	36	GENIC	homozygous	110930231
2	44969058	44969059	G	A	30	GENIC	homozygous	110692999
2	44969082	44969083	A	C	37	GENIC	homozygous	110508379
2	44969170	44969171	G	C	36	GENIC	homozygous	110693001
2	44969256	44969257	A		34	GENIC	possibly homozygous	130862146
2	44969206	44969206		GATT	37	GENIC	homozygous	130862144
2	44969246	44969247	C		40	GENIC	homozygous	130862145
2	44969457	44969458	G	A	37	GENIC	homozygous	110693003
2	44969614	44969614		GGCG	41	GENIC	homozygous	130862147
2	44970452	44970453	C	T	40	GENIC	homozygous	110508382
2	44971349	44971350	A		21	GENIC	homozygous	130862148
2	44972834	44972835	C	A	28	GENIC	homozygous	110508386
2	44973278	44973279	C	A	17	GENIC	homozygous	110508387
2	44973901	44973902	C	T	27	GENIC	homozygous	110508389
2	44979755	44979756	G	A	43	GENIC	heterozygous	110693005
2	44974051	44974052	C	T	32	GENIC	homozygous	110508390
2	44974458	44974459	A	G	36	GENIC	homozygous	110508391
2	44974473	44974474	A	G	38	GENIC	homozygous	110508392
2	44979797	44979798	G	A	37	GENIC	heterozygous	110508396
2	44980392	44980393	A	T	35	GENIC	homozygous	110508405
2	44971390	44971391	C	T	29	GENIC	homozygous	111408121
2	44979737	44979738	A	G	46	GENIC	heterozygous	109725787
2	44979738	44979739	A	G	46	GENIC	heterozygous	109725789
2	44979768	44979769	G	A	44	GENIC	heterozygous	109725791
2	44979807	44979808	C	T	34	GENIC	heterozygous	109725794