chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26363969	26363970	G	GAGGA	22	GENIC	homozygous	50147722
12	26364508	26364511	TTT	---	20	GENIC	homozygous	50147734
12	26365998	26365999	G	GT	5	GENIC	heterozygous	50298947
12	26371704	26371705	T	G	44	GENIC	heterozygous	50485112
12	26374541	26374542	G	T	44	GENIC	heterozygous	50373717
12	26378068	26378069	T	TTCTCTC	15	GENIC	homozygous	50147825
12	26378547	26378548	T	TATGA	14	GENIC	homozygous	50147829
12	26388446	26388447	T	G	36	GENIC	homozygous	50147871
12	26389768	26389769	C	A	39	GENIC	possibly homozygous	50147881
12	26389769	26389770	C	G	38	GENIC	homozygous	50147883
12	26390457	26390458	C	T	18	GENIC	heterozygous	50298987
12	26391717	26391718	A	-	6	GENIC	heterozygous	50467366
12	26398721	26398722	T	TGTG	46	GENIC	homozygous	50147905
12	26403188	26403189	A	ATGG	35	GENIC	homozygous	50485114
12	26403300	26403301	A	-	2	GENIC	homozygous	50147913
12	26406811	26406812	C	CT	21	GENIC	heterozygous	50299002
12	26406811	26406812	C	CTT	21	GENIC	heterozygous	50147921
12	26410340	26410341	A	-	39	GENIC	homozygous	50147933
12	26423660	26423661	G	A	75	GENIC	homozygous	50485116
12	26427464	26427465	C	CGT	9	GENIC	heterozygous	50147994
12	26427488	26427489	T	TGC	9	GENIC	heterozygous	50147996
12	26432550	26432551	T	C	40	GENIC	homozygous	50148012
12	26434769	26434770	C	T	45	GENIC	heterozygous	50373721