chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	44969082	44969083	A	C	10	GENIC	homozygous	110508379
2	44969346	44969347	C	G	24	GENIC	homozygous	110508380
2	44969372	44969373	C	T	26	GENIC	homozygous	110508381
2	44970452	44970453	C	T	17	GENIC	homozygous	110508382
2	44970578	44970579	T	G	31	GENIC	heterozygous	110508383
2	44970582	44970583	T	G	28	GENIC	heterozygous	110508384
2	44970586	44970587	T	G	27	GENIC	heterozygous	110508385
2	44972834	44972835	C	A	23	GENIC	homozygous	110508386
2	44973278	44973279	C	A	11	GENIC	homozygous	110508387
2	44973901	44973902	C	T	19	GENIC	homozygous	110508389
2	44974051	44974052	C	T	22	GENIC	homozygous	110508390
2	44974458	44974459	A	G	13	GENIC	homozygous	110508391
2	44974473	44974474	A	G	13	GENIC	homozygous	110508392
2	44976636	44976637	C	A	30	GENIC	heterozygous	111241596
2	44979768	44979769	G	A	36	GENIC	heterozygous	109725791
2	44979797	44979798	G	A	32	GENIC	heterozygous	110508396
2	44980392	44980393	A	T	15	GENIC	homozygous	110508405