chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	84052186	84052187	A	G	28	GENIC	homozygous	116069113
11	84054592	84054593	T	C	27	GENIC	heterozygous	118210165
11	84055501	84055502	G	A	26	GENIC	heterozygous	118226528
11	84055537	84055538	G	A	32	GENIC	heterozygous	118210166
11	84056006	84056007	G	T	32	GENIC	homozygous	116069115
11	84056471	84056472	C	T	12	GENIC	homozygous	116069117
11	84056762	84056763	T	C	33	GENIC	possibly homozygous	118210167
11	84056807	84056808	A	G	19	GENIC	heterozygous	118210168
11	84056819	84056820	G	A	13	GENIC	heterozygous	118210169
11	84056832	84056833	G	A	10	GENIC	heterozygous	118210170
11	84057438	84057439	G	T	16	GENIC	homozygous	116069119
11	84059005	84059006	A	G	31	GENIC	homozygous	116069121
11	84059268	84059269	G	A	24	GENIC	homozygous	116069123
11	84059340	84059341	G	A	39	GENIC	homozygous	116069125
11	84060009	84060010	A	G	30	GENIC	possibly homozygous	116069127
11	84060222	84060223	C	A	25	GENIC	homozygous	116069129
11	84060931	84060932	T	C	23	GENIC	heterozygous	118229628
11	84061264	84061265	G	A	33	GENIC	homozygous	116069131
11	84061921	84061922	G	A	45	GENIC	homozygous	116069133
11	84062649	84062650	A	G	40	GENIC	homozygous	116069135
11	84062668	84062669	C	A	43	GENIC	homozygous	116069137
11	84062823	84062824	A	C	38	GENIC	homozygous	116069139
11	84062979	84062980	C	T	44	GENIC	homozygous	116069141
11	84063169	84063170	G	A	28	GENIC	homozygous	118210171
11	84063213	84063214	A	G	20	GENIC	homozygous	118210172
11	84063578	84063579	A	G	18	GENIC	homozygous	116069143
11	84063775	84063776	T	A	16	GENIC	homozygous	116380911
11	84065405	84065406	C	T	27	GENIC	homozygous	116069145
11	84065610	84065611	T	C	40	GENIC	homozygous	116069147
11	84066408	84066409	C	T	23	GENIC	homozygous	116069149
11	84066800	84066801	A	T	35	GENIC	heterozygous	116421689
11	84067080	84067081	A	G	34	GENIC	homozygous	116069151
11	84067219	84067220	T	G	40	GENIC	heterozygous	118229629
11	84067398	84067399	A	T	25	GENIC	homozygous	116069153