chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	100881976	100881977	T	C	34	GENIC	homozygous	114437735
13	100883211	100883212	G	T	19	GENIC	homozygous	114437737
13	100883311	100883312	G	A	21	GENIC	possibly homozygous	114585077
13	100883321	100883322	G	A	20	GENIC	possibly homozygous	114585079
13	100883344	100883345	G	A	17	GENIC	homozygous	118467444
13	100883357	100883358	G	A	16	GENIC	homozygous	118467445
13	100883385	100883386	G	A	14	GENIC	homozygous	118467449
13	100883389	100883390	G	A	14	GENIC	homozygous	118467450
13	100883430	100883431	G	A	17	GENIC	homozygous	118467451
13	100883434	100883435	C	G	17	GENIC	homozygous	118467452
13	100883463	100883464	G	A	14	GENIC	homozygous	114437739
13	100883468	100883469	G	C	14	GENIC	homozygous	118467453
13	100883471	100883472	G	C	14	GENIC	homozygous	118467454
13	100883472	100883473	T	C	14	GENIC	homozygous	118467455
13	100883483	100883484	G	C	30	GENIC	homozygous	118467456
13	100884933	100884934	C	A	20	GENIC	homozygous	114437741
13	100884959	100884960	T	G	21	GENIC	homozygous	114437743
13	100885047	100885048	C	G	15	GENIC	homozygous	114437745
13	100885083	100885084	C	A	14	GENIC	homozygous	114585081
13	100883396	100883397	G	A	13	GENIC	homozygous	115017604
13	100883443	100883444	T	C	15	GENIC	possibly homozygous	115017606
13	100883422	100883423	G	A	14	GENIC	homozygous	115032953
13	100883445	100883446	T	C	15	GENIC	possibly homozygous	115032955
13	100885188	100885189	C	A	14	GENIC	homozygous	118467459
13	100885202	100885203	T	A	13	GENIC	homozygous	118467460
13	100885203	100885204	C	G	13	GENIC	homozygous	118467461
13	100885212	100885213	C	G	13	GENIC	homozygous	118467462
13	100885237	100885238	C	T	22	GENIC	homozygous	115017610
13	100885259	100885260	C	T	24	GENIC	homozygous	114990175