chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40730817	40730818	C	T	26	GENIC	homozygous	50204498
12	40732744	40732745	C	A	4	GENIC	homozygous	50543745
12	40733381	40733382	C	CA	6	GENIC	homozygous	50204499
12	40733714	40733715	T	TTAAATAAATAAA	3	GENIC	homozygous	50615570
12	40734944	40734946	AA	--	16	GENIC	possibly homozygous	50204501
12	40735512	40735513	T	C	18	GENIC	homozygous	50204502
12	40735904	40735905	T	C	29	GENIC	homozygous	50204503
12	40736456	40736457	A	G	22	GENIC	homozygous	50204504
12	40736765	40736766	A	G	21	GENIC	homozygous	50204505
12	40737243	40737244	G	T	7	GENIC	homozygous	50204506
12	40737256	40737257	A	G	6	GENIC	homozygous	50204507
12	40737262	40737263	G	C	5	GENIC	homozygous	50204508
12	40737268	40737269	C	T	5	GENIC	homozygous	50204509
12	40737595	40737596	C	T	26	GENIC	homozygous	50204515
12	40737871	40737872	T	A	24	GENIC	homozygous	50204516
12	40737889	40737890	T	C	19	GENIC	homozygous	50204517
12	40738207	40738208	C	T	30	GENIC	homozygous	50204518
12	40738324	40738325	G	T	22	GENIC	homozygous	50204519
12	40738404	40738405	C	A	19	GENIC	homozygous	50204520
12	40738602	40738603	G	GCGCGCGCACACACACACACA	14	GENIC	homozygous	50615571
12	40738857	40738858	C	T	30	GENIC	homozygous	50204522
12	40738965	40738966	C	T	23	GENIC	homozygous	50204523
12	40739314	40739315	G	-	8	GENIC	homozygous	50204524
12	40739343	40739348	TTTTT	-----	4	GENIC	homozygous	50204525
12	40739961	40739962	C	T	26	GENIC	homozygous	50204531