chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185122551151225512GA23GENIChomozygous620520998
185122578851225789AG27GENIChomozygous620520999
185122591751225918AG25GENIChomozygous620521000
185122608951226090GA25GENIChomozygous620521001
185122626151226262GT22GENIChomozygous620521002
185122636851226369GT30GENIChomozygous620521003
185122637151226372CT31GENIChomozygous620521004
185122638051226381GGTTGGAGCCCACAGTAATTC28GENIChomozygous738738440
185122655851226559TC26GENIChomozygous620521005
185122661651226617TC25GENIChomozygous620521006
185122661851226619GA24GENIChomozygous620521007
185122666551226666TC25GENIChomozygous620521008
185122668251226683GC24GENIChomozygous620521009
185122670551226706GC18GENIChomozygous620521010
185122673251226733AG16GENIChomozygous620521011
185122708051227081AG21GENIChomozygous620521012
185122733951227340TC26GENIChomozygous620521013
185122798951227990CCTTG19GENIChomozygous738738441
185122949451229495GGCACACACACA2GENICheterozygous738738442
185122949451229495GGCGCACACACACA2GENICheterozygous738738444
185122987351229874CCTTTATTTATTTA2GENIChomozygous738738447
185123018151230182GA20GENIChomozygous620521014
185123182451231825AG29GENIChomozygous620521015
185123333751233338GC12GENIChomozygous620521016
185123368851233689A-11GENIChomozygous738738449
185123504451235045AG37GENIChomozygous620521017
185123666751236668CA19GENIChomozygous620521018
185123780851237809TA7GENIChomozygous620521019
185123784151237842TTATTC12GENIChomozygous738738450
185123840051238401TC39GENIChomozygous620521020
185123980051239801GGA13GENIChomozygous738738451
185124000751240017TGTGTGTGTG----------7GENIChomozygous738738456
185124015151240152T-14GENIChomozygous738738458
185124015451240155TC14GENIChomozygous620521021
185124096151240962AG26GENIChomozygous620521022
185124149251241493C-14GENIChomozygous738738459
185124190851241909AG18GENIChomozygous620521023
185124321151243212GC7GENIChomozygous620521024
185124342451243425GA12GENIChomozygous620521025