chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266288154266288155TC7GENIChomozygous108637793
1266289392266289393CT15GENIChomozygous108637794
1266289753266289754AT14GENIChomozygous108637795
1266291379266291380TC14GENIChomozygous108637797
1266291508266291509AC6GENIChomozygous108637798
1266292207266292208TC15GENIChomozygous108637799
1266292799266292800AC15GENIChomozygous108637800
1266293380266293381TC12GENICpossibly homozygous108637801
1266295367266295368CT20GENIChomozygous108637804
1266297145266297146CT7GENIChomozygous108637807
1266297270266297271GA19GENIChomozygous108637808
1266298612266298613AT17GENIChomozygous108637809
1266299968266299969GA18GENIChomozygous108637811
1266302828266302829TA14GENIChomozygous108637825
1266302963266302964CT15GENIChomozygous108637826
1266303477266303478TC20GENIChomozygous108637827
1266304345266304346AG16GENIChomozygous108637828
1266305210266305211AG14GENIChomozygous108637829
1266306401266306402AG12GENIChomozygous108637830
1266306663266306664AG8GENIChomozygous108637831
1266306674266306675GA7GENIChomozygous108637832
1266307827266307828CT21GENIChomozygous108637833
1266311696266311697CA17GENIChomozygous108637836
1266311809266311810AG16GENIChomozygous108637837
1266314805266314806AC29GENIChomozygous108637844
1266316430266316431AG10GENIChomozygous108637845
1266316615266316616TC16GENIChomozygous108637846
1266316701266316702AT7GENIChomozygous108637847