chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4182308805182308806CT47GENIChomozygous57023398
4182309146182309147C-36GENIChomozygous57023399
4182310392182310393CT23GENIChomozygous57023400
4182311719182311720TG29GENIChomozygous57023401
4182312719182312720GGGT48GENICheterozygous57023402
4182312719182312720GGGTGT48GENICpossibly homozygous57023403
4182314427182314428AG17GENIChomozygous57023404
4182314532182314533GA30GENIChomozygous57023405
4182315061182315065AAAC----20GENIChomozygous57023406
4182315710182315711TC25GENIChomozygous57023407
4182316131182316132AG24GENIChomozygous57023408
4182316762182316763CT36GENIChomozygous57023409
4182317744182317745GA31GENIChomozygous57023410