chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31645429	31645430	G	A	27	GENIC	homozygous	115812270
11	31646010	31646011	T	G	33	GENIC	homozygous	115812272
11	31646225	31646226	T	C	41	GENIC	homozygous	115812274
11	31646638	31646639	C	T	19	GENIC	homozygous	115812276
11	31646936	31646937	T	C	35	GENIC	homozygous	115812278
11	31651547	31651548	T	A	22	GENIC	homozygous	115812280
11	31652476	31652477	G	A	38	GENIC	homozygous	115812282
11	31653461	31653462	T	A	23	GENIC	homozygous	115812284
11	31653688	31653689	G	A	23	GENIC	homozygous	115812286
11	31654571	31654572	A	T	36	GENIC	homozygous	115812288
11	31655178	31655179	G	A	36	GENIC	homozygous	115812290
11	31655365	31655366	A	T	23	GENIC	homozygous	115812292
11	31655521	31655522	G	A	20	GENIC	homozygous	115812294
11	31655615	31655616	T	G	40	GENIC	homozygous	115812296
11	31657243	31657244	G	A	40	GENIC	homozygous	115812298
11	31658443	31658444	A	G	50	GENIC	homozygous	115812300
11	31660001	31660002	T	C	32	GENIC	possibly homozygous	115812302
11	31664624	31664625	G	C	28	GENIC	homozygous	115812304
11	31666332	31666333	C	T	39	GENIC	homozygous	115812308