chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108148763881487639TA16GENIChomozygous570174225
108148766381487664AG15GENIChomozygous570174226
108148769881487699GA13GENIChomozygous570174227
108148869581488696GA12GENIChomozygous571921644
108148878581488791TCTATG------19GENIChomozygous710891901
108148923881489239GA17GENIChomozygous570174228
108148924281489243TC15GENIChomozygous570174229
108148934681489347TC21GENIChomozygous571921645
108148946981489470GA23GENIChomozygous570174230
108148956581489566GT16GENIChomozygous570174231
108148957181489572AT16GENIChomozygous570174232
108149009181490092AG15GENIChomozygous570174233
108149035981490360CT22GENIChomozygous571921646
108149092581490926AT18GENIChomozygous570174234
108149102281491023GA28GENIChomozygous570174235
108149107981491080AC33GENIChomozygous570174236
108149111981491120GA26GENIChomozygous570174237
108149120081491205AAAAA-----5GENIChomozygous710891903
108149135181491352AG25GENIChomozygous570174238
108149171281491713TTG16GENIChomozygous710891904
108149173681491737GT18GENIChomozygous570174239
108149177481491775AG17GENIChomozygous571921647
108149180481491805GA19GENIChomozygous571921648
108149215281492153CT23GENIChomozygous570174240
108149215881492159T-22GENIChomozygous710891905
108149256381492564GA11GENIChomozygous571921649
108149260381492604GA10GENIChomozygous571921650
108149289481492895AAT5GENICheterozygous710891906
108149289681492897A-5GENICheterozygous710891907
108149320681493207AG14GENIChomozygous570174241
108149340981493410A-25GENIChomozygous710891908
108149346981493470TC28GENIChomozygous570174242
108149380981493810TC29GENIChomozygous571921651
108149407581494076TC25GENIChomozygous570174243
108149451081494511GA21GENIChomozygous571921652
108149507081495074ACAC----3GENICheterozygous710891910
108149507281495074AC--3GENICheterozygous710891911
108149566181495662AG25GENIChomozygous570174244
108149585781495858GA18GENIChomozygous571921653
108149643181496432TC8GENIChomozygous570174245