chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122092445720924458C-6GENICheterozygous50107346
122092448720924488CT11GENICpossibly homozygous50107348
122092450820924509CCCT13GENICheterozygous50107350
122092450820924509CCCTCT13GENICheterozygous50286254
122092482420924826GT--14GENICheterozygous50107352
122092483320924845TGTGTGTGTGTC------------17GENICpossibly homozygous50107354
122092483520924836TTCTG20GENICheterozygous50107356
122092498720924988CT26GENIChomozygous50107358
122092499920925000GA26GENIChomozygous50107360
122092508920925090TC27GENIChomozygous50107362
122092541320925414AG17GENIChomozygous50107364
122092545420925455GA11GENIChomozygous50107366
122092627320926274TC15GENIChomozygous50107368
122092633020926331AAT16GENIChomozygous50107370
122092665620926657GGA12GENICheterozygous50107372
122092695620926962TAGGTT------12GENIChomozygous50107374
122092736920927370C-16GENIChomozygous50107376
122092757220927582AGAAAGAAAG----------7GENICpossibly homozygous50107378
122092758920927590GGAA8GENICheterozygous50107380
122092760820927610AG--10GENIChomozygous50107382
122092763120927632AAG10GENICheterozygous50107384
122092764420927645AG11GENICheterozygous50107390
122092770920927710AG8GENICpossibly homozygous50107392
122092773520927737AA--3GENICheterozygous50107398
122092784420927845TC13GENIChomozygous50107404
122092803820928039CT9GENIChomozygous50107406
122092832520928326CCT5GENICheterozygous50107408
122092832520928326CCTT5GENICheterozygous50107410
122092886020928861AT12GENIChomozygous50107412
122092946220929463TC11GENIChomozygous50107414
122093009220930093CT17GENIChomozygous50107416
122093023520930236AAT19GENIChomozygous50107418
122093063220930633CCT12GENIChomozygous50107420
122093073520930736GA22GENIChomozygous50107422
122093129020931291GT37GENICheterozygous50107424