chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4182308805182308806CT22GENIChomozygous57023398
4182309146182309147C-33GENIChomozygous57023399
4182310392182310393CT23GENIChomozygous57023400
4182311719182311720TG20GENIChomozygous57023401
4182311907182311908CCACAAAG8GENICheterozygous58408771
4182311907182311908CCACAAAGAG8GENICheterozygous58359597
4182312719182312720GGGT23GENICheterozygous57023402
4182312719182312720GGGTGT23GENICpossibly homozygous57023403
4182313879182313880TTTTCTTCTTCTTC2GENICheterozygous58359599
4182314427182314428AG16GENIChomozygous57023404
4182314532182314533GA21GENIChomozygous57023405
4182315061182315065AAAC----26GENIChomozygous57023406
4182315710182315711TC26GENIChomozygous57023407
4182316131182316132AG23GENIChomozygous57023408
4182316762182316763CT33GENIChomozygous57023409
4182317744182317745GA16GENIChomozygous57023410