chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	77848816	77848817	C	G	30	GENIC	homozygous	108871828
1	77849397	77849398	C	T	25	GENIC	homozygous	109294259
1	77850395	77850396	C	T	30	GENIC	possibly homozygous	109294261
1	77850709	77850710	T	A	30	GENIC	homozygous	108871831
1	77850951	77850952	A	G	31	GENIC	homozygous	108871832
1	77851184	77851185	A	T	25	GENIC	homozygous	109294263
1	77851309	77851310	C	G	31	GENIC	homozygous	109294265
1	77851546	77851547	C	A	16	GENIC	homozygous	109294266
1	77851722	77851723	G	A	17	GENIC	homozygous	108871834
1	77852567	77852568	G	C	42	GENIC	homozygous	109294268
1	77855891	77855892	A	G	35	GENIC	homozygous	109294270
1	77856415	77856416	T	C	45	GENIC	homozygous	108871841
1	77856557	77856558	T	A	34	GENIC	homozygous	109294272
1	77856734	77856735	T	C	37	GENIC	homozygous	108871842
1	77856753	77856754	A	G	39	GENIC	homozygous	108871843
1	77856942	77856943	C	T	32	GENIC	homozygous	108871844
1	77857346	77857347	T	C	62	GENIC	possibly homozygous	109294273
1	77857454	77857455	C	T	30	GENIC	homozygous	109294275
1	77857561	77857562	A	G	21	GENIC	homozygous	109294276
1	77857963	77857964	A	T	44	GENIC	homozygous	109294278
1	77858491	77858492	G	A	45	GENIC	homozygous	109294279
1	77858723	77858724	G	A	28	GENIC	homozygous	109294281
1	77858923	77858924	C	T	31	GENIC	possibly homozygous	109294283
1	77859487	77859488	G	A	25	GENIC	homozygous	108871847
1	77859996	77859997	C	T	8	GENIC	homozygous	109294285
1	77860249	77860250	G	A	33	GENIC	homozygous	109294287
1	77860545	77860546	C	T	18	GENIC	homozygous	109294289
1	77860784	77860785	T	C	28	GENIC	homozygous	108871851
1	77860991	77860992	T	C	33	GENIC	homozygous	108871852
1	77862388	77862389	A	G	23	GENIC	homozygous	108871853
1	77863131	77863132	G	T	40	GENIC	homozygous	108871854
1	77863873	77863874	A	C	37	GENIC	homozygous	109294291
1	77863887	77863888	C	T	37	GENIC	homozygous	109294293
1	77864705	77864706	T	G	10	GENIC	homozygous	108871855
1	77865270	77865271	C	G	30	GENIC	possibly homozygous	109294295