chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40588187	40588188	T	C	60	GENIC	homozygous	139143343
12	40589857	40589858	C	T	48	GENIC	homozygous	139143344
12	40590106	40590107	A	T	40	GENIC	homozygous	139143345
12	40590398	40590399	A	G	40	GENIC	homozygous	139143346
12	40591641	40591642	T	C	56	GENIC	homozygous	139143347
12	40592059	40592060	A	G	53	GENIC	homozygous	139143348
12	40592156	40592157	G	T	58	GENIC	homozygous	139143349
12	40593474	40593475	T	C	67	GENIC	possibly homozygous	139143350
12	40595077	40595078	G	C	48	GENIC	homozygous	139143351
12	40595415	40595419	CTCT		52	GENIC	homozygous	139056338
12	40595443	40595444	C	T	53	GENIC	homozygous	139143352
12	40595925	40595926	C	T	56	GENIC	homozygous	139143353
12	40596020	40596021	A		27	GENIC	heterozygous	403645805
12	40596018	40596019	G	A	27	GENIC	homozygous	154748902
12	40596018	40596019	G		27	GENIC	heterozygous	403645804
12	40596020	40596021	A	G	27	GENIC	homozygous	154748903
12	40596076	40596086	ACACACACGT		30	GENIC	homozygous	139056339
12	40596085	40596086	T		30	GENIC	homozygous	404021354
12	40596085	40596086	T	G	30	GENIC	heterozygous	404021355
12	40596667	40596668	C	T	46	GENIC	homozygous	139143354
12	40597223	40597224	G	A	58	GENIC	homozygous	139143355
12	40598393	40598394	T	C	50	GENIC	homozygous	139143356