chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101015341910153420AC9GENIChomozygous51616341
101015470010154701TC21GENIChomozygous51323997
101015506510155066CT21GENIChomozygous51323998
101015521310155214AG28GENIChomozygous51616342
101015527810155279CT16GENIChomozygous51616343
101015545410155455CT24GENIChomozygous51616344
101015557310155574GA13GENIChomozygous51616346
101015611010156111AT14GENIChomozygous51616347
101015653910156540CT15GENIChomozygous51616348
101015655110156552GA18GENIChomozygous51616349
101015669210156693AG23GENIChomozygous51324001
101015677410156775AG16GENIChomozygous51324002
101015680510156806GGTT14GENIChomozygous51324004
101015687810156879TC23GENIChomozygous51616350
101015706510157066AAC12GENIChomozygous51324007
101015711810157119AC12GENIChomozygous51616351
101015720510157222CATACATGTATTTATTT-----------------13GENICpossibly homozygous51324009
101015723110157237ACATAC------12GENICheterozygous51616356
101015729610157297TC28GENIChomozygous51616357
101015769810157699TC21GENIChomozygous51616358
101015799410157995AT14GENIChomozygous51616359
101015802510158026GA8GENICheterozygous52239165
101016125210161253CCA7GENICheterozygous51616360
101016265410162655GC13GENIChomozygous51616361
101016277110162772GA26GENIChomozygous51616362
101016300910163010AG15GENIChomozygous51616364
101016330910163310GA24GENIChomozygous51324016
101016353310163534TC18GENIChomozygous51324017
101016422310164224GGAA14GENICheterozygous51324018
101016422310164224GGA14GENICheterozygous51324019
101016422310164224GGAAA14GENICheterozygous51616366
101015554610155551GGTTC-----8GENICheterozygous52480735
101016422310164224GGAAAA14GENICheterozygous52480739
101015701610157017T-2GENICheterozygous52718611
101015720510157207CA--13GENICheterozygous52354933
101016125310161255AA--7GENICheterozygous51803674
101016295510162967GCGCGCGCGCGC------------4GENICheterozygous53329049