chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	240629350	240629351	T	C	24	GENIC	homozygous	110334630
2	240629441	240629442	G	A	21	GENIC	homozygous	110843359
2	240629475	240629476	T	C	26	GENIC	homozygous	110334632
2	240630554	240630555	C	A	19	GENIC	homozygous	110334636
2	240631488	240631489	C	A	21	GENIC	homozygous	110843360
2	240631606	240631607	T	C	13	GENIC	homozygous	110334638
2	240631792	240631793	G	T	24	GENIC	homozygous	111289883
2	240631800	240631801	T	G	27	GENIC	homozygous	110632342
2	240632450	240632451	T	A	25	GENIC	homozygous	110334640
2	240633185	240633186	T	C	31	GENIC	homozygous	110843361
2	240633212	240633213	A	T	40	GENIC	homozygous	110334642
2	240635319	240635320	C	T	29	GENIC	homozygous	110843362
2	240636763	240636764	G	A	25	GENIC	possibly homozygous	110334652
2	240637067	240637068	A	G	19	GENIC	homozygous	110843363
2	240640971	240640972	C	A	22	GENIC	homozygous	110843364
2	240642611	240642612	A	T	27	GENIC	possibly homozygous	120161907
2	240642780	240642781	G	T	24	GENIC	homozygous	110334662
2	240645839	240645840	G	A	20	GENIC	homozygous	110334666
2	240646082	240646083	G	A	27	GENIC	homozygous	110334668
2	240646549	240646550	G	A	28	GENIC	homozygous	110334670
2	240647279	240647280	A	G	31	GENIC	homozygous	110334672
2	240647404	240647405	C	T	25	GENIC	homozygous	110334674
2	240647967	240647968	C	T	34	GENIC	homozygous	110334676
2	240649670	240649671	C	A	21	GENIC	possibly homozygous	110843365
2	240650194	240650195	A	G	22	GENIC	homozygous	110334678
2	240651673	240651674	A	G	21	GENIC	homozygous	110334682
2	240652833	240652834	A	C	29	GENIC	homozygous	110334684
2	240653324	240653325	A	G	20	GENIC	homozygous	110843366