chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	84650502	84650503	A	G	28	GENIC	homozygous	112758248
4	84650632	84650633	T	G	38	GENIC	homozygous	112758250
4	84650856	84650857	C	T	19	GENIC	homozygous	112758252
4	84651347	84651348	T	C	25	GENIC	homozygous	112758254
4	84651414	84651415	C	A	30	GENIC	homozygous	119278747
4	84651415	84651416	A	G	30	GENIC	homozygous	112758256
4	84651549	84651550	G	A	39	GENIC	homozygous	112758258
4	84651897	84651898	G	A	22	GENIC	homozygous	112758260
4	84652125	84652126	G	A	48	GENIC	homozygous	112758262
4	84652389	84652390	T	A	8	GENIC	possibly homozygous	112758264
4	84652965	84652966	C	T	22	GENIC	homozygous	112758266
4	84653012	84653013	T	C	31	GENIC	homozygous	112758268
4	84653078	84653079	C	T	49	GENIC	homozygous	112758270
4	84653085	84653086	T	A	53	GENIC	homozygous	112758272
4	84653627	84653628	G	A	57	GENIC	homozygous	112758274
4	84653954	84653955	C	T	17	GENIC	homozygous	112758276
4	84654010	84654011	T	A	12	GENIC	homozygous	119278749
4	84654654	84654655	C	G	48	GENIC	homozygous	119278751
4	84654675	84654676	A	G	48	GENIC	homozygous	112758278
4	84654714	84654715	A	G	43	GENIC	homozygous	112758280
4	84654924	84654925	A	G	36	GENIC	possibly homozygous	112758282
4	84655031	84655032	A	G	20	GENIC	homozygous	112758284
4	84655072	84655073	T	C	17	GENIC	homozygous	112758286
4	84655129	84655130	T	C	19	GENIC	homozygous	112758288
4	84655647	84655648	A	G	30	GENIC	homozygous	112758290
4	84655694	84655695	A	G	45	GENIC	possibly homozygous	112758292
4	84655966	84655967	G	A	39	GENIC	homozygous	112758294
4	84655967	84655968	G	A	39	GENIC	homozygous	112758296
4	84656040	84656041	G	A	30	GENIC	homozygous	112758298
4	84656141	84656142	C	T	33	GENIC	homozygous	112758300
4	84656242	84656243	G	A	26	GENIC	homozygous	112758302
4	84656382	84656383	C	T	66	GENIC	homozygous	112758304
4	84656384	84656385	T	C	64	GENIC	homozygous	112758306
4	84656473	84656474	T	C	43	GENIC	homozygous	112758308
4	84656534	84656535	T	G	46	GENIC	homozygous	112758310