chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30880472	30880473	T	C	16	GENIC	homozygous	116096109
11	30880650	30880651	A	G	30	GENIC	homozygous	115809846
11	30881286	30881287	T	C	39	GENIC	homozygous	116096111
11	30882026	30882027	G	A	30	GENIC	homozygous	115959985
11	30882936	30882937	T	C	12	GENIC	possibly homozygous	115959986
11	30883071	30883072	A	G	12	GENIC	homozygous	116096113
11	30883155	30883156	T	A	12	GENIC	homozygous	116096115
11	30883216	30883217	T	C	19	GENIC	homozygous	115809852
11	30883314	30883315	G	C	50	GENIC	homozygous	116096117
11	30883384	30883385	G	C	90	GENIC	heterozygous	118192321
11	30883419	30883420	G	C	63	GENIC	homozygous	118192322
11	30883424	30883425	C	T	59	GENIC	possibly homozygous	118192323
11	30883484	30883485	A	C	72	GENIC	heterozygous	118192324
11	30883560	30883561	T	C	10	GENIC	homozygous	118192326
11	30883587	30883588	T	A	11	GENIC	heterozygous	118192327
11	30884111	30884112	A	G	21	GENIC	homozygous	116096119
11	30884206	30884207	T	C	23	GENIC	homozygous	116096121
11	30884486	30884487	A	G	23	GENIC	homozygous	115809854
11	30886157	30886158	C	T	21	GENIC	homozygous	115809858
11	30886612	30886613	G	C	23	GENIC	homozygous	116096123
11	30886629	30886630	A	G	24	GENIC	homozygous	115809860
11	30886858	30886859	A	G	19	GENIC	homozygous	116096125
11	30887179	30887180	T	C	36	GENIC	homozygous	115809862
11	30887639	30887640	T	C	20	GENIC	homozygous	116096127
11	30889474	30889475	T	C	37	GENIC	homozygous	115959988
11	30889480	30889481	A	G	36	GENIC	homozygous	115809866
11	30889986	30889987	A	G	27	GENIC	possibly homozygous	116096129
11	30890039	30890040	G	A	14	GENIC	possibly homozygous	118192329
11	30890081	30890082	T	G	8	GENIC	possibly homozygous	115809872
11	30890808	30890809	A	G	22	GENIC	homozygous	116096131
11	30890862	30890863	G	A	26	GENIC	homozygous	116096133
11	30891923	30891924	T	A	11	GENIC	homozygous	115959989
11	30893243	30893244	G	T	30	GENIC	homozygous	116096135
11	30883723	30883724	T	A	23	GENIC	heterozygous	118198628