chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126784622126784623AG16GENIChomozygous113998782
5126785192126785193TC15GENIChomozygous113998784
5126786891126786892GA9GENIChomozygous113998786
5126787730126787731GA9GENICheterozygous113998788
5126789564126789565TC18GENIChomozygous113998790
5126790951126790952GC25GENIChomozygous113998792
5126791002126791003GA19GENIChomozygous113998794
5126791083126791084GA16GENIChomozygous113998796
5126791180126791181GA18GENIChomozygous113998798
5126791374126791375TC20GENIChomozygous114137417
5126791616126791617CT20GENIChomozygous114137418
5126791673126791674GA15GENIChomozygous113998808
5126791737126791738CA28GENIChomozygous113998811
5126791888126791889CG10GENIChomozygous114137419
5126791891126791892CG8GENIChomozygous114137420
5126791900126791901GT10GENIChomozygous113998819
5126792521126792522TC20GENIChomozygous113998827
5126792661126792662AG25GENIChomozygous113998829
5126793181126793182GA14GENIChomozygous113998831
5126794490126794491CT18GENIChomozygous113998833
5126796861126796862AT23GENIChomozygous113998835
5126798209126798210CA31GENIChomozygous113998839
5126798351126798352AG25GENIChomozygous113998841
5126798646126798647CT23GENIChomozygous113998843
5126798816126798817GA13GENIChomozygous113998845
5126799502126799503TC31GENIChomozygous113998847
5126800146126800147GA13GENIChomozygous113998849
5126800424126800425CT14GENIChomozygous113998851
5126801073126801074GA24GENIChomozygous113998853
5126802364126802365CA17GENIChomozygous113998855
5126802943126802944AG10GENIChomozygous113998857