chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40730273	40730274	C	T	16	GENIC	homozygous	50422955
12	40732744	40732745	C	A	1	GENIC	homozygous	50543745
12	40733381	40733382	C	CA	5	GENIC	heterozygous	50204499
12	40733381	40733382	C	CAA	5	GENIC	heterozygous	50323380
12	40733655	40733656	C	T	12	GENIC	homozygous	50422956
12	40734272	40734273	C	T	28	GENIC	homozygous	50422957
12	40735512	40735513	T	C	12	GENIC	homozygous	50204502
12	40735729	40735733	ATCT	----	6	GENIC	homozygous	50543746
12	40735904	40735905	T	C	23	GENIC	homozygous	50204503
12	40736664	40736665	G	A	15	GENIC	homozygous	50422959
12	40736765	40736766	A	G	22	GENIC	homozygous	50204505
12	40737243	40737244	G	T	14	GENIC	homozygous	50204506
12	40737308	40737309	C	CAAAA	2	GENIC	heterozygous	50422960
12	40737488	40737489	C	A	15	GENIC	homozygous	50422961
12	40739346	40739348	TT	--	5	GENIC	heterozygous	50422962
12	40739347	40739348	T	-	5	GENIC	heterozygous	50422963
12	40739541	40739542	C	CTT	10	GENIC	homozygous	50204527
12	40739851	40739852	T	A	15	GENIC	homozygous	50422964
12	40739961	40739962	C	T	26	GENIC	homozygous	50204531
12	40740345	40740346	G	A	20	GENIC	homozygous	50422965