chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124345841124345842TA5GENIChomozygous883578526
7124346015124346016TC20GENIChomozygous883578525
7124346975124346976AG16GENIChomozygous883578524
7124347454124347455GA10GENICheterozygous883578523
7124349087124349088AC26GENIChomozygous883578522
7124352089124352090AG5GENICheterozygous883578521
7124354042124354043AG4GENIChomozygous883578520
7124354541124354542AG17GENIChomozygous883578519
7124355740124355741TC6GENIChomozygous883578518
7124356690124356691AT4GENICheterozygous883578517
7124357260124357261GA13GENIChomozygous883578516
7124357588124357589GA23GENIChomozygous883578515
7124357875124357876GA11GENIChomozygous883578514
7124358195124358196GA26GENIChomozygous883578513
7124359640124359641GA13GENIChomozygous883578512
7124360476124360477CT20GENIChomozygous883578511
7124362633124362634GA20GENIChomozygous883578510
7124363341124363342CA21GENIChomozygous883578509
7124364483124364484CT10GENIChomozygous883578508
7124366143124366144AG27GENIChomozygous883578507
7124366322124366323GA16GENIChomozygous883578506
7124367434124367435GT24GENIChomozygous883578505