chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	33179865	33179866	A	G	35	GENIC	homozygous	115455370
6	33180921	33180922	C	A	14	GENIC	homozygous	115455371
6	33181599	33181600	T	A	15	GENIC	possibly homozygous	115455372
6	33182488	33182489	A	C	19	GENIC	homozygous	115455373
6	33183549	33183550	A	G	13	GENIC	possibly homozygous	114756830
6	33183554	33183555	T	C	14	GENIC	possibly homozygous	114756832
6	33183898	33183899	T	A	18	GENIC	homozygous	115455374
6	33184796	33184797	C	T	21	GENIC	homozygous	115455375
6	33185269	33185270	T	C	9	GENIC	homozygous	115455376
6	33186368	33186369	A	G	16	GENIC	possibly homozygous	115455377
6	33186734	33186735	G	T	28	GENIC	homozygous	115455378
6	33187435	33187436	A	G	19	GENIC	homozygous	115455379
6	33192999	33193000	A	G	16	GENIC	homozygous	115455380
6	33197186	33197187	G	T	9	GENIC	homozygous	115455381
6	33198165	33198166	T	C	17	GENIC	possibly homozygous	115455382
6	33198706	33198707	G	A	18	GENIC	homozygous	115455383
6	33200275	33200276	T	C	9	GENIC	homozygous	115455384
6	33204164	33204165	A	T	15	GENIC	homozygous	115455385
6	33206291	33206292	C	A	21	GENIC	homozygous	115455386
6	33206381	33206382	G	A	24	GENIC	homozygous	115455387
6	33208778	33208779	C	T	17	GENIC	homozygous	115455388
6	33209160	33209161	T	C	27	GENIC	homozygous	115455389
6	33209537	33209538	T	G	22	GENIC	homozygous	115455390
6	33210038	33210039	G	A	15	GENIC	homozygous	115455391
6	33210353	33210354	C	T	18	GENIC	homozygous	115455392
6	33211460	33211461	C	T	20	GENIC	homozygous	115455393
6	33211477	33211478	T	C	20	GENIC	homozygous	115455394
6	33213202	33213203	A	G	13	GENIC	homozygous	115455395
6	33213464	33213465	A	G	27	GENIC	homozygous	115455396
6	33215424	33215425	T	C	13	GENIC	homozygous	115455397
6	33215478	33215479	T	G	24	GENIC	homozygous	115455398