chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479664	42479665	T		25	GENIC	homozygous	128991452
12	42480898	42480899	G	A	59	GENIC	homozygous	115331360
12	42482185	42482186	C	A	19	GENIC	homozygous	115331364
12	42486020	42486024	ATAC		30	GENIC	homozygous	128991453
12	42486920	42486921	T		27	GENIC	homozygous	128991454
12	42487728	42487729	T	C	31	GENIC	homozygous	115331366
12	42488221	42488222	T	C	10	GENIC	homozygous	115442482
12	42488240	42488240		CT	4	GENIC	homozygous	128991455
12	42488458	42488458		T	28	GENIC	homozygous	128991457
12	42489556	42489557	C	T	48	GENIC	homozygous	115331368
12	42490416	42490417	A	G	71	GENIC	homozygous	115331370
12	42492457	42492458	T	C	21	GENIC	homozygous	115331372
12	42493812	42493813	T	A	54	GENIC	homozygous	115331374
12	42494137	42494138	C	G	53	GENIC	possibly homozygous	115331376
12	42494137	42494137		TG	50	GENIC	homozygous	128991459
12	42494398	42494399	C	T	53	GENIC	homozygous	115331378
12	42494466	42494467	A	G	63	GENIC	homozygous	115331380
12	42494491	42494492	A	G	53	GENIC	homozygous	115331382