chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	4422573	4422574	T	A	27	GENIC	homozygous	117669898
9	4422574	4422575	T	A	26	GENIC	homozygous	117669900
9	4424782	4424783	A	G	28	GENIC	possibly homozygous	117208461
9	4431140	4431141	A	G	24	GENIC	homozygous	117669904
9	4434682	4434683	A	G	21	GENIC	possibly homozygous	117208482
9	4434683	4434684	A	C	21	GENIC	possibly homozygous	117208483
9	4434796	4434797	T	G	26	GENIC	heterozygous	117208484
9	4434803	4434804	C	T	29	GENIC	heterozygous	117208485
9	4434811	4434812	T	C	25	GENIC	heterozygous	117208486
9	4434812	4434813	G	A	25	GENIC	heterozygous	117208487
9	4434840	4434841	G	A	34	GENIC	heterozygous	117208488
9	4435119	4435120	A	C	29	GENIC	heterozygous	117208489
9	4435581	4435582	C	T	34	GENIC	heterozygous	117208490
9	4435615	4435616	G	A	35	GENIC	heterozygous	117208491
9	4435632	4435633	G	A	38	GENIC	heterozygous	117208492
9	4435637	4435638	C	T	37	GENIC	heterozygous	117208493
9	4435658	4435659	T	G	35	GENIC	heterozygous	117208494
9	4435664	4435665	A	C	37	GENIC	heterozygous	117208495
9	4435671	4435672	T	C	37	GENIC	heterozygous	117208496
9	4435724	4435725	C	T	47	GENIC	heterozygous	117208497
9	4435807	4435808	T	A	38	GENIC	heterozygous	117208498
9	4435850	4435851	G	A	31	GENIC	heterozygous	117474534
9	4435854	4435855	C	G	29	GENIC	heterozygous	117474536