chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	12378623	12378623		T	26	GENIC	heterozygous	128960724
12	12384482	12384483	A	G	24	GENIC	homozygous	115258345
12	12384510	12384511	G	A	25	GENIC	homozygous	115416394
12	12386254	12386255	T	C	24	GENIC	homozygous	115258349
12	12387667	12387668	C	T	37	GENIC	homozygous	115258351
12	12387685	12387686	C	T	35	GENIC	homozygous	115258353
12	12390457	12390458	A	G	33	GENIC	homozygous	115258355
12	12390505	12390506	T	C	29	GENIC	homozygous	115258357
12	12392016	12392017	T	C	41	GENIC	homozygous	115258359
12	12393171	12393172	T	C	21	GENIC	homozygous	115258361
12	12394607	12394608	T	C	18	GENIC	homozygous	115258363
12	12394924	12394924		TAT	18	GENIC	possibly homozygous	128960728
12	12396325	12396328	ATA		31	GENIC	homozygous	128960729
12	12396330	12396338	GAAAGAGA		31	GENIC	homozygous	128960730
12	12398929	12398930	G	A	34	GENIC	homozygous	115258367
12	12400198	12400199	C	T	24	GENIC	homozygous	115416398
12	12400739	12400740	A	G	23	GENIC	homozygous	115258373
12	12400948	12400948		TGGGGCTGGGGATT	15	GENIC	homozygous	128960731
12	12402722	12402723	T	C	35	GENIC	homozygous	115258377
12	12403144	12403145	C		28	GENIC	homozygous	128960732