chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24099350	24099351	T	C	18	GENIC	heterozygous	50131371
12	24110251	24110252	G	A	85	GENIC	heterozygous	51141735
12	24112092	24112093	A	G	7	GENIC	heterozygous	50131564
12	24115903	24115904	G	T	26	GENIC	heterozygous	50589115
12	24120193	24120194	T	C	49	GENIC	heterozygous	50292542
12	24120877	24120878	T	G	12	GENIC	heterozygous	50292551
12	24121013	24121014	T	C	24	GENIC	heterozygous	50292553
12	24121022	24121023	C	T	24	GENIC	heterozygous	50292555
12	24121098	24121099	A	G	24	GENIC	heterozygous	50292557
12	24121539	24121540	C	T	37	GENIC	heterozygous	50292571
12	24121540	24121541	A	G	37	GENIC	heterozygous	50292573
12	24121549	24121550	C	T	44	GENIC	heterozygous	51141736
12	24121550	24121551	G	A	45	GENIC	heterozygous	50292575
12	24122063	24122064	G	-	9	GENIC	heterozygous	50292600
12	24122068	24122069	G	A	7	GENIC	heterozygous	50292602
12	24133655	24133656	T	C	10	GENIC	heterozygous	50131682
12	24134409	24134410	G	T	23	GENIC	heterozygous	50292634
12	24134410	24134411	A	G	23	GENIC	heterozygous	50292636
12	24134565	24134566	C	T	37	GENIC	heterozygous	50131684
12	24134579	24134580	G	A	36	GENIC	heterozygous	50131686