chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	166998911	166998912	A	G	23	GENIC	homozygous	108357374
1	166999047	166999048	C	T	31	GENIC	heterozygous	108357375
1	166999479	166999480	T	C	38	GENIC	possibly homozygous	108357376
1	166999495	166999496	C	T	48	GENIC	possibly homozygous	108357377
1	167000311	167000312	A	G	39	GENIC	homozygous	108357378
1	167000479	167000480	G	A	47	GENIC	homozygous	108357379
1	167001076	167001077	C	T	40	GENIC	homozygous	108357380
1	167002104	167002105	G	C	43	GENIC	homozygous	108357381
1	167002745	167002746	T	A	45	GENIC	homozygous	108357382
1	167003507	167003508	T	C	37	GENIC	homozygous	108357383
1	167004963	167004964	T	A	44	GENIC	possibly homozygous	108357384
1	167005470	167005471	T	C	8	GENIC	possibly homozygous	108357385
1	167005513	167005514	A	T	12	GENIC	possibly homozygous	108357386
1	167005559	167005560	A	G	8	GENIC	homozygous	108357387
1	167005568	167005569	T	C	14	GENIC	possibly homozygous	108357388
1	167007763	167007764	A	C	21	GENIC	homozygous	108357389
1	167009316	167009317	C	T	45	GENIC	homozygous	108357390
1	167009532	167009533	T	C	34	GENIC	homozygous	108357391
1	167009857	167009858	T	C	37	GENIC	homozygous	108357392
1	167010011	167010012	G	A	53	GENIC	homozygous	108357393
1	167010017	167010018	A	G	47	GENIC	homozygous	108357394
1	167011312	167011313	C	T	36	GENIC	homozygous	108357395
1	167011313	167011314	A	G	36	GENIC	homozygous	108357396
1	167011419	167011420	A	G	42	GENIC	homozygous	108357397
1	167011457	167011458	A	G	43	GENIC	homozygous	108357398
1	167011955	167011956	T	G	27	GENIC	possibly homozygous	108357399
1	167013183	167013184	C	T	43	GENIC	possibly homozygous	108357400
1	167013631	167013632	G	A	29	GENIC	homozygous	108357401
1	167014379	167014380	A	C	48	GENIC	homozygous	108357402
1	167014491	167014492	C	T	60	GENIC	homozygous	108357403
1	167014574	167014575	C	A	47	GENIC	homozygous	108357404