chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	27130571	27130571		GGTTT	76	GENIC	homozygous	128893475
11	27130842	27130842		A	65	GENIC	homozygous	128893476
11	27131115	27131116	G		47	GENIC	heterozygous	128893477
11	27135208	27135209	A	G	62	GENIC	homozygous	115799147
11	27135354	27135355	A	C	44	GENIC	homozygous	115799149
11	27136465	27136465		G	72	GENIC	homozygous	128893478
11	27137222	27137223	A	T	66	GENIC	homozygous	116033055
11	27132806	27132807	A	C	67	GENIC	possibly homozygous	116033047
11	27136131	27136132	C	A	67	GENIC	homozygous	116033049
11	27136487	27136488	T	C	68	GENIC	homozygous	116033051
11	27136657	27136658	G	A	53	GENIC	homozygous	116033053
11	27137293	27137294	A	G	64	GENIC	homozygous	115799151
11	27137625	27137626	G	T	71	GENIC	possibly homozygous	115799153
11	27139725	27139726	A	C	63	GENIC	possibly homozygous	115799155
11	27141371	27141372	C	T	62	GENIC	homozygous	115799159
11	27141054	27141057	AAT		79	GENIC	homozygous	131103801