chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	44968927	44968928	A	G	47	GENIC	homozygous	110692997
2	44968936	44968937	T	C	48	GENIC	homozygous	110930229
2	44968937	44968938	G	C	49	GENIC	homozygous	110930230
2	44968939	44968940	C	T	48	GENIC	homozygous	110930231
2	44969058	44969059	G	A	45	GENIC	homozygous	110692999
2	44969082	44969083	A	C	38	GENIC	homozygous	110508379
2	44969170	44969171	G	C	38	GENIC	homozygous	110693001
2	44969256	44969257	A		35	GENIC	homozygous	130862146
2	44969206	44969206		GATT	39	GENIC	homozygous	130862144
2	44969246	44969247	C		41	GENIC	homozygous	130862145
2	44969457	44969458	G	A	31	GENIC	possibly homozygous	110693003
2	44969614	44969614		GGCG	28	GENIC	homozygous	130862147
2	44970452	44970453	C	T	39	GENIC	homozygous	110508382
2	44971349	44971350	A		23	GENIC	homozygous	130862148
2	44972834	44972835	C	A	41	GENIC	homozygous	110508386
2	44973278	44973279	C	A	19	GENIC	homozygous	110508387
2	44973901	44973902	C	T	43	GENIC	homozygous	110508389
2	44974051	44974052	C	T	41	GENIC	homozygous	110508390
2	44974458	44974459	A	G	45	GENIC	homozygous	110508391
2	44974473	44974474	A	G	43	GENIC	homozygous	110508392
2	44979797	44979798	G	A	37	GENIC	heterozygous	110508396
2	44980392	44980393	A	T	26	GENIC	possibly homozygous	110508405
2	44971390	44971391	C	T	35	GENIC	homozygous	111408121
2	44979737	44979738	A	G	47	GENIC	heterozygous	109725787
2	44979738	44979739	A	G	47	GENIC	heterozygous	109725789
2	44979768	44979769	G	A	50	GENIC	heterozygous	109725791
2	44979807	44979808	C	T	38	GENIC	heterozygous	109725794