chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23655112	23655113	C	A	28	GENIC	homozygous	115446091
12	23655279	23655280	A	G	24	GENIC	homozygous	115446093
12	23655635	23655636	A	G	32	GENIC	homozygous	115446095
12	23656356	23656357	T	C	18	GENIC	homozygous	115446097
12	23656426	23656427	A	C	33	GENIC	homozygous	115446099
12	23656540	23656541	A	G	12	GENIC	homozygous	115446101
12	23656556	23656557	A	G	15	GENIC	homozygous	115446103
12	23656603	23656604	G	A	32	GENIC	homozygous	115446105
12	23656694	23656695	C	T	28	GENIC	homozygous	115446107
12	23656894	23656895	T	C	19	GENIC	homozygous	115446109
12	23656910	23656911	G	T	19	GENIC	homozygous	115446111
12	23657233	23657234	G	A	29	GENIC	homozygous	115446113
12	23657869	23657870	A	C	34	GENIC	homozygous	115285396
12	23657978	23657979	C	G	26	GENIC	homozygous	115446115
12	23658065	23658066	G	A	20	GENIC	homozygous	115446117
12	23658194	23658195	T	C	21	GENIC	homozygous	115285406
12	23658338	23658339	C	G	28	GENIC	homozygous	115446119
12	23658464	23658465	C	G	41	GENIC	homozygous	115446121
12	23658572	23658573	T	C	35	GENIC	homozygous	115285414
12	23658573	23658574	G	A	35	GENIC	homozygous	115285416
12	23658626	23658627	G	T	29	GENIC	homozygous	115285418
12	23658783	23658784	G	A	30	GENIC	homozygous	115285420
12	23659497	23659498	A	C	20	GENIC	homozygous	115285422
12	23660709	23660710	C	T	24	GENIC	homozygous	115285426
12	23660739	23660740	G	A	27	GENIC	homozygous	115285428