chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23752887	23752888	A	T	22	GENIC	homozygous	115438455
12	23753517	23753518	A	C	24	GENIC	possibly homozygous	115438456
12	23753648	23753649	C	T	13	GENIC	possibly homozygous	118324917
12	23755402	23755403	T	C	20	GENIC	homozygous	115285704
12	23755560	23755561	C	T	18	GENIC	possibly homozygous	118261859
12	23755564	23755565	C	T	18	GENIC	homozygous	118261860
12	23755608	23755609	C	T	20	GENIC	homozygous	115703393
12	23755612	23755613	C	T	19	GENIC	homozygous	118301135
12	23755616	23755617	C	T	19	GENIC	homozygous	118301136
12	23758913	23758914	G	A	13	GENIC	heterozygous	118324918
12	23758919	23758920	T	C	13	GENIC	heterozygous	118261861
12	23758929	23758930	G	A	12	GENIC	heterozygous	118261862
12	23758934	23758935	G	A	11	GENIC	heterozygous	118261863
12	23759565	23759566	G	T	29	GENIC	homozygous	115438457
12	23759579	23759580	C	A	27	GENIC	homozygous	115438458
12	23759925	23759926	A	G	33	GENIC	homozygous	115438459
12	23760289	23760290	G	C	15	GENIC	homozygous	115438460
12	23760808	23760809	T	C	12	GENIC	homozygous	115285722
12	23760818	23760819	T	C	14	GENIC	homozygous	115285724
12	23760916	23760917	G	C	11	GENIC	homozygous	115285726
12	23761317	23761318	A	G	19	GENIC	homozygous	115438461
12	23762535	23762536	A	G	22	GENIC	homozygous	115285730
12	23763717	23763718	C	T	20	GENIC	homozygous	115438463
12	23765221	23765222	C	T	21	GENIC	homozygous	115484878
12	23765345	23765346	A	G	29	GENIC	homozygous	115285738
12	23768599	23768600	G	A	18	GENIC	homozygous	115368630
12	23769020	23769021	A	G	13	GENIC	homozygous	118301140
12	23769326	23769327	T	C	23	GENIC	homozygous	115285760