chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224127833224127834CT20GENICpossibly homozygous57109338
4224128443224128444CCT2GENICheterozygous58376139
4224128755224128756AC10GENICheterozygous57109345
4224129798224129799GA21GENICpossibly homozygous57109347
4224131195224131196CT2GENIChomozygous57109353
4224132197224132198A-2GENICheterozygous57109357
4224132200224132202AA--4GENICheterozygous57109360
4224133177224133178TC13GENICpossibly homozygous57109364
4224135484224135485TTCTAGCAGTTATTCTCTTTGC4GENIChomozygous57109368
4224135658224135659GA7GENIChomozygous57109372
4224135909224135910GA10GENIChomozygous57109373
4224136700224136701AAT17GENIChomozygous57109379
4224137618224137619C-10GENICpossibly homozygous57109381
4224138806224138807GGA12GENIChomozygous57109392
4224138899224138900TG14GENICpossibly homozygous57109394
4224138946224138947AG3GENICheterozygous57109396
4224138963224138964TG6GENIChomozygous57109398
4224139285224139286AT13GENIChomozygous57109400
4224139696224139697AG7GENIChomozygous57109402
4224140065224140066CT18GENICpossibly homozygous57109409
4224140240224140241GT24GENIChomozygous57109411