chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31643000	31643001	G	A	39	GENIC	heterozygous	118141577
11	31643217	31643218	G	A	33	GENIC	homozygous	116129297
11	31644533	31644534	G	T	122	GENIC	heterozygous	118141579
11	31644583	31644584	T	C	139	GENIC	heterozygous	118141580
11	31644600	31644601	T	A	120	GENIC	heterozygous	118141582
11	31644809	31644810	A	G	64	GENIC	heterozygous	118141584
11	31644898	31644899	G	A	79	GENIC	heterozygous	118141585
11	31644901	31644902	A	G	82	GENIC	heterozygous	118141587
11	31646638	31646639	C	T	42	GENIC	homozygous	115812276
11	31646010	31646011	T	G	38	GENIC	homozygous	115812272
11	31645429	31645430	G	A	36	GENIC	homozygous	115812270
11	31646225	31646226	T	C	49	GENIC	possibly homozygous	115812274
11	31646936	31646937	T	C	66	GENIC	possibly homozygous	115812278
11	31649945	31649946	G	A	34	GENIC	heterozygous	118141589
11	31651547	31651548	T	A	37	GENIC	possibly homozygous	115812280
11	31652476	31652477	G	A	66	GENIC	homozygous	115812282
11	31653461	31653462	T	A	42	GENIC	homozygous	115812284
11	31653688	31653689	G	A	44	GENIC	homozygous	115812286
11	31654571	31654572	A	T	55	GENIC	homozygous	115812288
11	31655178	31655179	G	A	38	GENIC	homozygous	115812290
11	31655365	31655366	A	T	54	GENIC	homozygous	115812292
11	31655521	31655522	G	A	51	GENIC	homozygous	115812294
11	31655615	31655616	T	G	49	GENIC	homozygous	115812296
11	31656642	31656643	A	C	45	GENIC	homozygous	118141590
11	31657243	31657244	G	A	46	GENIC	homozygous	115812298
11	31658068	31658069	C	T	11	GENIC	heterozygous	118141592
11	31658071	31658072	G	A	15	GENIC	possibly homozygous	118141593
11	31658085	31658086	G	A	23	GENIC	possibly homozygous	118141595
11	31658089	31658090	G	C	24	GENIC	possibly homozygous	118141597
11	31658056	31658057	G	A	10	GENIC	heterozygous	116314288
11	31658443	31658444	A	G	55	GENIC	homozygous	115812300
11	31660001	31660002	T	C	48	GENIC	homozygous	115812302
11	31664624	31664625	G	C	81	GENIC	homozygous	115812304
11	31666332	31666333	C	T	61	GENIC	homozygous	115812308