chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115512383115512384CT23GENICheterozygous53167601
8115513030115513031CT15GENICheterozygous52826279
8115516330115516331CCG37GENICheterozygous52826286
8115518076115518077AG21GENICheterozygous52826290
8115519250115519251GA10GENICheterozygous52826293
8115523834115523835AG56GENICheterozygous53167625
8115527949115527950AC10GENICheterozygous52826307
8115527950115527951GA10GENICheterozygous52826308
8115539897115539898TTG10GENICheterozygous53167634
8115541589115541590AAG23GENICheterozygous52826326
8115555931115555932CT43GENICheterozygous53167652
8115583690115583691CT12GENICheterozygous53050341
8115583713115583714C-10GENICheterozygous53050343
8115587025115587026CT30GENICheterozygous53167670
8115592854115592855AG9GENICheterozygous52826461
8115616477115616478AG17GENICheterozygous52826507
8115622529115622531CT--19GENICheterozygous53167692
8115626308115626309AT15GENICheterozygous53167694
8115632810115632812CC--10GENICheterozygous52826515
8115632953115632954CT44GENICheterozygous53167704
8115639625115639626TA9GENICheterozygous52826516