chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	10536946	10536947	T	C	26	GENIC	homozygous	114722349
6	10537065	10537066	C	T	44	GENIC	homozygous	114722351
6	10538013	10538014	G	A	30	GENIC	homozygous	114722353
6	10538361	10538362	C	G	24	GENIC	homozygous	114722355
6	10538571	10538572	T	C	27	GENIC	homozygous	114722357
6	10538600	10538601	A	G	29	GENIC	homozygous	114722359
6	10538602	10538603	T	G	29	GENIC	homozygous	114722361
6	10538607	10538608	A	G	29	GENIC	homozygous	114722363
6	10539671	10539672	G	T	21	GENIC	homozygous	114722365
6	10540219	10540220	A	G	31	GENIC	possibly homozygous	114722367
6	10540394	10540395	C	T	19	GENIC	possibly homozygous	114722371
6	10540512	10540513	A	C	18	GENIC	homozygous	114722373
6	10540791	10540792	T	C	15	GENIC	homozygous	114722375
6	10540962	10540963	A	G	12	GENIC	homozygous	114722377
6	10542336	10542337	C	T	35	GENIC	homozygous	114722379
6	10542383	10542384	A	C	33	GENIC	possibly homozygous	114722381
6	10542855	10542856	G	A	28	GENIC	homozygous	114722383
6	10543588	10543589	C	A	30	GENIC	homozygous	114722385
6	10545685	10545686	G	A	31	GENIC	homozygous	114722389
6	10546145	10546146	T	C	13	GENIC	homozygous	114722391
6	10547793	10547794	C	T	28	GENIC	homozygous	114722393
6	10548857	10548858	G	A	39	GENIC	possibly homozygous	114722395
6	10549319	10549320	T	C	26	GENIC	homozygous	114722397
6	10551136	10551137	C	T	32	GENIC	homozygous	114722399
6	10551228	10551229	T	C	23	GENIC	homozygous	114722401
6	10551346	10551347	G	A	33	GENIC	homozygous	114722403
6	10551623	10551624	C	T	27	GENIC	homozygous	114722405
6	10551996	10551997	A	G	34	GENIC	homozygous	114722407
6	10552009	10552010	T	C	31	GENIC	homozygous	114722409
6	10552021	10552022	A	G	29	GENIC	homozygous	114722411
6	10553191	10553192	C	T	17	GENIC	homozygous	114722413
6	10567369	10567370	A	G	38	GENIC	heterozygous	115090139
6	10567378	10567379	A	G	38	GENIC	heterozygous	115090140
6	10567417	10567418	T	A	32	GENIC	heterozygous	115090141