chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	82001217	82001218	T	C	11	GENIC	homozygous	52762184
9	82002371	82002372	A	G	28	GENIC	homozygous	52762186
9	82003083	82003084	A	G	25	GENIC	homozygous	52762189
9	82003525	82003526	G	A	24	GENIC	homozygous	52762192
9	82003740	82003741	G	A	27	GENIC	homozygous	52762195
9	82004206	82004207	T	TG	23	GENIC	possibly homozygous	52762198
9	82004749	82004750	C	T	25	GENIC	homozygous	52762200
9	82004781	82004782	T	C	18	GENIC	homozygous	52762203
9	82005042	82005064	CCATCAGCCACTGTATAACCTC	----------------------	8	GENIC	heterozygous	52952948
9	82005363	82005364	T	C	23	GENIC	homozygous	52268462
9	82005574	82005575	A	G	24	GENIC	possibly homozygous	52762211
9	82006194	82006195	A	C	17	GENIC	homozygous	52762214
9	82006336	82006337	A	T	25	GENIC	homozygous	52762217
9	82006375	82006376	T	C	31	GENIC	homozygous	52762220
9	82006636	82006637	C	CTCTGTGATATAGT	23	GENIC	homozygous	52762223
9	82007938	82007939	C	T	15	GENIC	homozygous	52762229
9	82008285	82008286	T	C	10	GENIC	homozygous	52762232
9	82008361	82008362	T	C	13	GENIC	homozygous	52762235
9	82008403	82008404	A	G	14	GENIC	homozygous	52762238
9	82008407	82008408	G	T	15	GENIC	homozygous	52762241