chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3117469144117469145CT41GENIChomozygous57620425
3117470844117470845CCT12GENICheterozygous57620427
3117473201117473202GA13GENICheterozygous57620429
3117474490117474491AG29GENIChomozygous57620431
3117475471117475472TTA39GENIChomozygous57620433
3117477746117477747TG44GENICheterozygous57620435
3117477801117477802TG26GENICheterozygous57620437
3117478517117478518TG30GENICheterozygous57620439
3117478575117478576AAG5GENIChomozygous57620441
3117478965117478966GA51GENIChomozygous57620443
3117479469117479470T-18GENIChomozygous57620445
3117479994117479995T-9GENICheterozygous57620447
3117482649117482650AG38GENIChomozygous57620449
3117483450117483451AG17GENIChomozygous57620451
3117486673117486674AAT36GENICpossibly homozygous57620453
3117487117117487118A-5GENIChomozygous57620455
3117487617117487618C-6GENICheterozygous57620457
3117488395117488396TC21GENIChomozygous57620459
3117490342117490343CCT22GENICpossibly homozygous57620461