chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479664	42479665	T		6	GENIC	homozygous	128991452
12	42480898	42480899	G	A	14	GENIC	homozygous	115331360
12	42482185	42482186	C	A	8	GENIC	homozygous	115331364
12	42486020	42486024	ATAC		6	GENIC	homozygous	128991453
12	42486920	42486921	T		11	GENIC	homozygous	128991454
12	42487728	42487729	T	C	19	GENIC	homozygous	115331366
12	42488221	42488222	T	C	5	GENIC	homozygous	115442482
12	42488307	42488308	C		4	GENIC	homozygous	128991456
12	42488458	42488458		T	7	GENIC	homozygous	128991457
12	42489556	42489557	C	T	18	GENIC	homozygous	115331368
12	42490416	42490417	A	G	18	GENIC	homozygous	115331370
12	42492457	42492458	T	C	4	GENIC	homozygous	115331372
12	42493812	42493813	T	A	22	GENIC	homozygous	115331374
12	42494137	42494138	C	G	14	GENIC	homozygous	115331376
12	42494137	42494137		TG	14	GENIC	homozygous	128991459
12	42494398	42494399	C	T	12	GENIC	homozygous	115331378
12	42494466	42494467	A	G	18	GENIC	homozygous	115331380
12	42494491	42494492	A	G	18	GENIC	homozygous	115331382