chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24593013	24593014	A	T	9	GENIC	homozygous	115422284
12	24593021	24593022	A	G	7	GENIC	homozygous	115422286
12	24593243	24593244	C	T	13	GENIC	homozygous	115422288
12	24593460	24593461	G	A	10	GENIC	homozygous	115422290
12	24593490	24593491	T	C	10	GENIC	homozygous	115422292
12	24593531	24593532	T	C	16	GENIC	homozygous	115288423
12	24594263	24594264	T	C	15	GENIC	homozygous	115422294
12	24594659	24594660	C	G	8	GENIC	homozygous	115422296
12	24594709	24594710	C	T	10	GENIC	homozygous	115288429
12	24595060	24595061	A	C	8	GENIC	homozygous	115288433
12	24595200	24595201	C	T	14	GENIC	homozygous	115288435
12	24595260	24595261	C	T	15	GENIC	homozygous	115288437
12	24595584	24595585	G	A	24	GENIC	homozygous	115288439
12	24595915	24595916	T	A	4	GENIC	homozygous	115485110
12	24596916	24596917	G	A	14	GENIC	homozygous	115288443
12	24597261	24597262	A	G	18	GENIC	homozygous	115288447
12	24597762	24597763	C	T	16	GENIC	homozygous	115422302
12	24597770	24597771	C	T	16	GENIC	homozygous	115422304
12	24597837	24597838	C	T	30	GENIC	homozygous	115422306
12	24598059	24598060	T	C	15	GENIC	homozygous	115288449
12	24598104	24598105	T	C	23	GENIC	homozygous	115288451
12	24598824	24598825	T	C	27	GENIC	homozygous	115288455
12	24598974	24598975	T	C	11	GENIC	homozygous	115288457
12	24600022	24600023	T	A	14	GENIC	homozygous	115422308
12	24601356	24601357	T	C	17	GENIC	homozygous	115288459
12	24602751	24602752	A	T	15	GENIC	homozygous	115288461
12	24605990	24605991	A	T	10	GENIC	homozygous	115493095
12	24614926	24614927	C	G	23	GENIC	homozygous	115288501
12	24617056	24617057	T	C	13	GENIC	homozygous	115288515