chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7887107678871077TC7GENIChomozygous108277332
X7887142278871423TC12GENIChomozygous108804639
X7887450978874510CT13GENIChomozygous108277336
X7887548278875483CT7GENIChomozygous108277338
X7887626278876262T10GENIChomozygous129758213
X7887766378877665TA9GENICpossibly homozygous129758217
X7887920078879201CG12GENIChomozygous108277342
X7887945478879455TC12GENIChomozygous108804641
X7888405678884057GT6GENIChomozygous108277348
X7888655778886558CT16GENIChomozygous108804643
X7888753078887531CA14GENIChomozygous108804645
X7889236778892368TC7GENIChomozygous108277354
X7889467478894675TC9GENIChomozygous108277356
X7889810978898110AG11GENIChomozygous108277360
X7887637678876377GC4GENICheterozygous108686081
X7887510178875101AGATAAA12GENIChomozygous129758210
X7887619178876191AGG9GENIChomozygous129758211
X7887620178876202C9GENIChomozygous129758212
X7887638178876382AG4GENICheterozygous135284675
X7890023578900236CA6GENICheterozygous135284676
X7887891278878912G8GENIChomozygous135244196
X7888409878884099CT8GENIChomozygous108818219
X7889774178897742AG11GENIChomozygous108620201
X7890214978902150TC7GENIChomozygous108277362
X7890273178902732A11GENIChomozygous129758220
X7890440678904407GC14GENIChomozygous108620203
X7890477778904778GA8GENIChomozygous108277366
X7890607178906072AG12GENIChomozygous108277368
X7890752878907529GT17GENIChomozygous108277370
X7890905078909051GA7GENIChomozygous108804647
X7891061178910612GA17GENIChomozygous108804649
X7891062978910629AA12GENIChomozygous135244197
X7891068878910689CG4GENIChomozygous108804651
X7891125378911255AA10GENIChomozygous129758222
X7890398678903987CT7GENIChomozygous108677351