chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31834992	31834994	AA		37	GENIC	possibly homozygous	132885134
11	31835011	31835012	A		33	GENIC	heterozygous	128896282
11	31835709	31835710	T	C	76	GENIC	homozygous	115812590
11	31836441	31836442	G	A	44	GENIC	homozygous	115812594
11	31839878	31839879	T	G	42	GENIC	homozygous	115812602
11	31842127	31842128	A	C	49	GENIC	homozygous	115812608
11	31842129	31842130	A	G	49	GENIC	homozygous	115812610
11	31844267	31844269	AC		22	GENIC	heterozygous	132885135
11	31844271	31844272	C		22	GENIC	heterozygous	132885136
11	31844274	31844275	C		22	GENIC	heterozygous	132885137
11	31838130	31838131	G	A	48	GENIC	homozygous	116178439
11	31838603	31838604	G	A	51	GENIC	homozygous	116178441
11	31840298	31840299	C	T	33	GENIC	homozygous	116178443
11	31844927	31844928	T	G	37	GENIC	heterozygous	134021464
11	31845882	31845883	C	T	56	GENIC	homozygous	116178445