chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224127833224127834CT18GENICpossibly homozygous57109338
4224128755224128756AC19GENICpossibly homozygous57109345
4224129798224129799GA24GENIChomozygous57109347
4224131156224131157TTAC6GENICheterozygous57109351
4224131195224131196CT9GENICheterozygous57109353
4224132197224132198A-1GENIChomozygous57109357
4224132200224132202AA--2GENIChomozygous57109360
4224133177224133178TC19GENICheterozygous57109364
4224135484224135485TTCTAGCAGTTATTCTCTTTGC1GENIChomozygous57109368
4224135658224135659GA15GENIChomozygous57109372
4224135909224135910GA17GENICpossibly homozygous57109373
4224136700224136701AAT17GENIChomozygous57109379
4224137618224137619C-11GENIChomozygous57109381
4224138806224138807GGA14GENIChomozygous57109392
4224138899224138900TG17GENICheterozygous57109394
4224138946224138947AG12GENIChomozygous57109396
4224138963224138964TG10GENICpossibly homozygous57109398
4224139285224139286AT15GENICpossibly homozygous57109400
4224139696224139697AG4GENIChomozygous57109402
4224140065224140066CT27GENIChomozygous57109409
4224140240224140241GT25GENICpossibly homozygous57109411