chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	82000717	82000718	C	T	28	GENIC	homozygous	53450473
9	82002237	82002238	G	A	34	GENIC	homozygous	53450476
9	82002371	82002372	A	G	37	GENIC	possibly homozygous	52762186
9	82004206	82004207	T	TGGGG	5	GENIC	heterozygous	52268458
9	82004781	82004782	T	C	34	GENIC	homozygous	52762203
9	82005042	82005064	CCATCAGCCACTGTATAACCTC	----------------------	15	GENIC	homozygous	52952948
9	82005363	82005364	T	C	27	GENIC	homozygous	52268462
9	82006336	82006337	A	T	27	GENIC	homozygous	52762217
9	82006636	82006637	C	CTCTGTGATATAGT	31	GENIC	homozygous	52762223
9	82007674	82007675	A	AGG	16	GENIC	homozygous	53450479
9	82007758	82007759	G	C	31	GENIC	homozygous	53450482
9	82007938	82007939	C	T	21	GENIC	homozygous	52762229
9	82008285	82008286	T	C	24	GENIC	homozygous	52762232
9	82008361	82008362	T	C	21	GENIC	homozygous	52762235
9	82008403	82008404	A	G	29	GENIC	homozygous	52762238