chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40732744	40732745	C	A	6	GENIC	homozygous	50543745
12	40732747	40732755	AAAAAAAA	--------	8	GENIC	heterozygous	50949194
12	40734944	40734946	AA	--	17	GENIC	homozygous	50204501
12	40735233	40735234	C	T	35	GENIC	homozygous	50949197
12	40735704	40735705	C	CATCT	11	GENIC	homozygous	50323382
12	40735904	40735905	T	C	22	GENIC	homozygous	50204503
12	40736664	40736665	G	A	23	GENIC	homozygous	50422959
12	40737243	40737244	G	T	17	GENIC	homozygous	50204506
12	40737308	40737309	C	CAAAAAA	7	GENIC	heterozygous	50543747
12	40737308	40737309	C	CAAAA	7	GENIC	heterozygous	50422960
12	40738602	40738603	G	GCACA	17	GENIC	homozygous	50640206
12	40739302	40739303	G	GAAA	11	GENIC	homozygous	50571771
12	40739346	40739348	TT	--	9	GENIC	heterozygous	50422962
12	40739347	40739348	T	-	9	GENIC	heterozygous	50422963
12	40739541	40739542	C	CT	13	GENIC	homozygous	50452380
12	40739851	40739852	T	A	23	GENIC	homozygous	50422964
12	40739961	40739962	C	T	20	GENIC	homozygous	50204531
12	40740345	40740346	G	A	29	GENIC	homozygous	50422965