chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	161654874	161654875	A	G	31	GENIC	homozygous	108342451
1	161655576	161655577	C	G	18	GENIC	homozygous	108951375
1	161655732	161655733	T	C	40	GENIC	homozygous	108951376
1	161655839	161655840	C	A	30	GENIC	homozygous	108951377
1	161656424	161656425	G	A	32	GENIC	homozygous	108951378
1	161658850	161658851	G	C	25	GENIC	homozygous	108342457
1	161658851	161658852	G	A	25	GENIC	homozygous	108951379
1	161660267	161660268	C	T	27	GENIC	homozygous	108951380
1	161663054	161663055	T	G	31	GENIC	homozygous	108951381
1	161663629	161663630	G	A	21	GENIC	homozygous	108951382
1	161663741	161663742	T	A	27	GENIC	homozygous	108951383
1	161664142	161664143	G	A	28	GENIC	homozygous	108951384
1	161665729	161665730	T	A	27	GENIC	homozygous	108951385
1	161665739	161665740	A	G	24	GENIC	homozygous	108342459
1	161667374	161667375	T	C	18	GENIC	homozygous	108342461
1	161668160	161668161	C	A	33	GENIC	homozygous	108951386
1	161669189	161669190	G	A	39	GENIC	homozygous	108951387
1	161670578	161670579	C	T	20	GENIC	homozygous	108951388
1	161671142	161671143	T	C	22	GENIC	possibly homozygous	108951389
1	161671673	161671674	T	C	27	GENIC	homozygous	108951390
1	161672763	161672764	T	G	23	GENIC	homozygous	108951391
1	161673174	161673175	T	C	19	GENIC	homozygous	108951392
1	161673485	161673486	C	T	35	GENIC	homozygous	108951393
1	161677874	161677875	A	C	27	GENIC	homozygous	108951394
1	161677954	161677955	C	T	22	GENIC	homozygous	108951395
1	161675702	161675703	A	G	61	GENIC	heterozygous	109051768