chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	84041901	84041902	G	A	40	GENIC	possibly homozygous	116069066
11	84042146	84042147	A	G	37	GENIC	homozygous	116069068
11	84042198	84042199	A	G	42	GENIC	homozygous	116069071
11	84042507	84042508	T	C	24	GENIC	homozygous	118210161
11	84042524	84042524		CGCT	22	GENIC	homozygous	132157790
11	84042529	84042531	AT		22	GENIC	homozygous	132157791
11	84043119	84043120	C	T	22	GENIC	homozygous	116069073
11	84043127	84043128	C	T	24	GENIC	homozygous	116069075
11	84044072	84044073	G	A	29	GENIC	homozygous	116069077
11	84044170	84044171	G	C	20	GENIC	homozygous	116069079
11	84044171	84044172	G	C	20	GENIC	homozygous	116069081
11	84044202	84044203	C	G	19	GENIC	homozygous	116069083
11	84044934	84044935	T	A	29	GENIC	homozygous	116069085
11	84045112	84045113	G	C	37	GENIC	homozygous	116069087
11	84046697	84046698	A		26	GENIC	homozygous	132157792
11	84046713	84046723	AAAAATATAT		29	GENIC	possibly homozygous	132157793
11	84046705	84046706	A	T	28	GENIC	possibly homozygous	116267239
11	84046037	84046038	A	G	36	GENIC	homozygous	116069089
11	84046183	84046184	T	G	24	GENIC	homozygous	116069091
11	84046487	84046488	C	T	30	GENIC	homozygous	116069093
11	84047391	84047392	C	T	24	GENIC	homozygous	116069095
11	84043930	84043931	C	A	14	GENIC	homozygous	116250148
11	84043941	84043942	A	G	14	GENIC	homozygous	116207739
11	84046688	84046689	A	T	26	GENIC	homozygous	116207741
11	84046692	84046693	A	T	28	GENIC	homozygous	116207743
11	84047408	84047409	C	G	25	GENIC	homozygous	116207745
11	84046679	84046680	A		24	GENIC	homozygous	128930462