chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95066956050669561GC20GENIChomozygous126515716
95067220650672207GA14GENIChomozygous126552350
95067660250676603TA3GENICheterozygous126607445
95068120250681203GA9GENICheterozygous126515720
95068151950681520CT10GENIChomozygous126515722
95068167950681680CT13GENIChomozygous126515724
95068254750682548TC13GENIChomozygous126515726
95069014650690147CT18GENIChomozygous126515732
95069907950699080GA9GENIChomozygous126515734
95069910350699104CT7GENIChomozygous126552351
95070097450700975AC10GENICheterozygous126552352
95070261750702618CT10GENIChomozygous126515736
95070571850705719TC27GENIChomozygous126515738
95070574450705745TC24GENIChomozygous126515740
95070618450706185AG24GENIChomozygous126515742
95070651250706513AG29GENIChomozygous126515744
95070866950708670GA14GENIChomozygous126515746
95071592450715925CT5GENICheterozygous117335020
95071926650719267TC17GENIChomozygous117540572
95071414850714149CT8GENIChomozygous117540568
95071690850716909GA13GENIChomozygous117540570
95072523450725235GT15GENIChomozygous117540574
95072644750726448TG18GENIChomozygous117540576
95072960250729603TG14GENIChomozygous117540578
95073049050730491GA18GENIChomozygous117540580
95074042850740429AC25GENIChomozygous117540586
95074050450740505CT18GENIChomozygous117540588
95074052150740522CT17GENIChomozygous117540590
95074073850740739GC23GENIChomozygous117540592
95074319750743198GA4GENICheterozygous117823061
95074391550743916AG17GENIChomozygous117540594
95074464750744648GA19GENIChomozygous117540596