chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107510286575102866GA19GENIChomozygous126462261
107510358175103582AG24GENICpossibly homozygous116638192
107510363075103631AG20GENIChomozygous116638194
107510479675104797AG5GENIChomozygous126462262
107510543775105438AT16GENIChomozygous116638198
107510617575106176AC16GENIChomozygous116638204
107510621675106217CT14GENIChomozygous116638206
107510760875107609TG17GENIChomozygous118001579
107510789775107898GA18GENICheterozygous116638210
107510815375108154TC12GENIChomozygous116638214
107510818175108182AG12GENIChomozygous116638216
107510821175108212AG14GENIChomozygous116638218
107510892375108924CT19GENIChomozygous126462263
107510972675109727TC13GENIChomozygous116638222
107511057475110575AG24GENIChomozygous116638228
107511091875110919TC13GENIChomozygous126462264
107511099875110999CT24GENIChomozygous116638229
107511116075111161TC29GENIChomozygous116638231
107511174775111748GA11GENIChomozygous116638233
107511180775111808AT19GENIChomozygous116638235
107511267875112679GA11GENIChomozygous116638237
107511300875113009CG4GENIChomozygous126462265
107511356675113567GA26GENICpossibly homozygous126462266
107511395875113959TC15GENIChomozygous116638239
107511403775114038GA21GENIChomozygous116638241
107511440275114403GA20GENIChomozygous116638243
107511553075115531GA19GENIChomozygous116638245
107511555175115552TA15GENIChomozygous116638247
107511620875116209TC22GENIChomozygous117065552
107511626475116265GA28GENIChomozygous117065554
107511631775116318GA24GENIChomozygous116638253
107511736975117370GA17GENIChomozygous116638255
107511759175117592CT6GENIChomozygous116638257
107511811475118115GA19GENIChomozygous116638259
107511822175118222TG15GENIChomozygous116638261
107511870275118703CG15GENIChomozygous116638263
107511871675118717CG8GENIChomozygous116638265
107511881575118816CA11GENIChomozygous117065558
107511904975119050AC25GENIChomozygous116638267
107512020875120209AG23GENIChomozygous116638269