chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	10975449	10975450	G	C	23	GENIC	heterozygous	113250962
4	10976256	10976257	T	C	10	GENIC	homozygous	112497368
4	10976502	10976503	G	A	18	GENIC	homozygous	112497370
4	10977752	10977753	C	G	23	GENIC	possibly homozygous	112497374
4	10977823	10977824	T	C	20	GENIC	heterozygous	112497376
4	10978080	10978081	G	A	23	GENIC	possibly homozygous	112497378
4	10978094	10978095	A	C	19	GENIC	homozygous	112497380
4	10978642	10978643	G	A	21	GENIC	homozygous	112497384
4	10978836	10978837	A	G	24	GENIC	homozygous	112497386
4	10978994	10978995	C	T	21	GENIC	homozygous	112497388
4	10979119	10979120	G	A	11	GENIC	homozygous	112497390
4	10979417	10979418	G	C	9	GENIC	possibly homozygous	112497392
4	10979611	10979612	C	T	38	GENIC	homozygous	112497394
4	10980871	10980872	A	G	25	GENIC	homozygous	112497396
4	10981022	10981023	T	C	31	GENIC	homozygous	112497398
4	10981333	10981334	C	T	38	GENIC	homozygous	112497400
4	10981504	10981505	C	T	52	GENIC	homozygous	112497402
4	10981763	10981764	C	T	21	GENIC	homozygous	112497404
4	10982020	10982021	T	G	29	GENIC	homozygous	112497406
4	10982329	10982330	C	A	37	GENIC	homozygous	112497408
4	10982339	10982340	T	C	38	GENIC	homozygous	112497410
4	10982694	10982695	A	G	60	GENIC	homozygous	112497412
4	10982762	10982763	C	T	70	GENIC	homozygous	112497414
4	10983051	10983052	C	A	41	GENIC	homozygous	112497416
4	10983072	10983073	C	T	51	GENIC	heterozygous	112497418
4	10983074	10983075	C	T	50	GENIC	heterozygous	112497420
4	10983304	10983305	G	T	17	GENIC	homozygous	112497422
4	10983435	10983436	C	T	31	GENIC	homozygous	112497424
4	10984084	10984085	T	G	48	GENIC	possibly homozygous	112497426
4	10984125	10984126	T	C	48	GENIC	possibly homozygous	112497428
4	10984477	10984478	C	T	18	GENIC	homozygous	112497430
4	10984659	10984660	T	C	21	GENIC	homozygous	112497432
4	10985226	10985227	T	A	53	GENIC	homozygous	112497434
4	10985310	10985311	C	G	51	GENIC	homozygous	112497436