chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	39115181	39115182	T	C	34	GENIC	homozygous	114760875
6	39115355	39115356	A	C	27	GENIC	homozygous	114760877
6	39115543	39115544	A	G	38	GENIC	homozygous	114760879
6	39115635	39115636	C	T	35	GENIC	homozygous	114760881
6	39115893	39115894	C	A	24	GENIC	homozygous	114760883
6	39116245	39116246	C	A	20	GENIC	homozygous	114760885
6	39116304	39116305	C	T	28	GENIC	homozygous	114760887
6	39118439	39118440	A	T	31	GENIC	homozygous	114760891
6	39120582	39120583	T	A	22	GENIC	homozygous	114760893
6	39122851	39122852	T	C	29	GENIC	homozygous	114760897
6	39123109	39123110	C	T	31	GENIC	homozygous	114760899
6	39124369	39124370	C	G	18	GENIC	homozygous	114760901
6	39125687	39125688	C	T	15	GENIC	homozygous	114760903
6	39126984	39126985	A	G	34	GENIC	homozygous	114760905
6	39127275	39127276	G	T	8	GENIC	homozygous	118595506
6	39127277	39127278	C	T	8	GENIC	homozygous	118595507
6	39127283	39127284	C	T	2	GENIC	homozygous	118595508
6	39128235	39128236	T	C	27	GENIC	homozygous	114760911
6	39128371	39128372	C	T	27	GENIC	homozygous	114760913
6	39128565	39128566	G	A	30	GENIC	homozygous	114760915
6	39129063	39129064	G	A	26	GENIC	homozygous	114760917
6	39129461	39129462	G	T	22	GENIC	homozygous	114760919
6	39129662	39129663	G	T	16	GENIC	homozygous	114760921
6	39129675	39129676	C	T	12	GENIC	homozygous	114760923
6	39130472	39130473	A	G	15	GENIC	homozygous	114760925
6	39130657	39130658	T	C	23	GENIC	homozygous	114760927
6	39130660	39130661	A	G	23	GENIC	homozygous	114760929
6	39130966	39130967	A	T	29	GENIC	homozygous	114760931
6	39131052	39131053	G	A	40	GENIC	homozygous	114760933
6	39131881	39131882	T	C	18	GENIC	homozygous	114760935
6	39131897	39131898	G	C	20	GENIC	homozygous	114760937
6	39132000	39132001	T	C	28	GENIC	homozygous	114760939
6	39132462	39132463	G	A	31	GENIC	homozygous	114760941
6	39133209	39133210	A	G	23	GENIC	homozygous	114760943
6	39133944	39133945	T	A	15	GENIC	homozygous	118552981
6	39134793	39134794	G	A	23	GENIC	homozygous	114760945