chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	118979792	118979793	C	G	22	GENIC	homozygous	109994568
2	118980116	118980117	C	T	40	GENIC	possibly homozygous	109994569
2	118980282	118980283	C	T	33	GENIC	possibly homozygous	109994571
2	118980386	118980387	G	A	25	GENIC	homozygous	109994573
2	118980952	118980953	C	T	31	GENIC	homozygous	109994575
2	118981308	118981309	A	G	36	GENIC	possibly homozygous	109994576
2	118981332	118981333	G	C	35	GENIC	possibly homozygous	109994578
2	118981395	118981396	T	C	18	GENIC	homozygous	109994580
2	118981530	118981531	C	A	21	GENIC	possibly homozygous	110968119
2	118981597	118981598	T	C	23	GENIC	homozygous	109994582
2	118981705	118981706	G	A	24	GENIC	homozygous	109994584
2	118982179	118982180	A	C	21	GENIC	homozygous	109994586
2	118983051	118983052	A	G	17	GENIC	homozygous	109994588
2	118983056	118983057	A	T	19	GENIC	homozygous	109994590
2	118989280	118989281	C	T	26	GENIC	homozygous	109994605
2	118989445	118989446	C	T	31	GENIC	possibly homozygous	109994607
2	118990152	118990153	G	A	19	GENIC	homozygous	109994609
2	118990762	118990763	C	T	20	GENIC	homozygous	109994611
2	118991445	118991446	C	T	23	GENIC	homozygous	109994613
2	119000638	119000639	T	C	26	GENIC	homozygous	109994615
2	119000695	119000696	G	A	23	GENIC	homozygous	109994617
2	119000729	119000730	G	A	24	GENIC	homozygous	109994619
2	119000859	119000860	T	C	18	GENIC	homozygous	109994621
2	119001275	119001276	A	T	19	GENIC	homozygous	109994623
2	119001658	119001659	G	A	11	GENIC	homozygous	109994625
2	119002176	119002177	C	T	19	GENIC	homozygous	120126576
2	119002177	119002178	T	C	18	GENIC	homozygous	120126577
2	119004617	119004618	A	G	26	GENIC	homozygous	109994633
2	119006663	119006664	A	G	11	GENIC	homozygous	109994634
2	119007402	119007403	A	G	33	GENIC	homozygous	109994636
2	119007758	119007759	T	C	18	GENIC	homozygous	109994638