chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139690012139690013CT19GENIChomozygous803073792
5139693004139693005GA7GENICheterozygous803073793
5139694090139694091GA15GENICheterozygous803073794
5139694279139694280AC32GENIChomozygous803073795
5139694442139694443GA25GENIChomozygous803073796
5139694920139694921CT12GENIChomozygous803073797
5139696549139696550AG25GENIChomozygous803073798
5139697356139697357CT23GENIChomozygous803073799
5139697456139697457AT24GENIChomozygous803073800
5139697670139697671GA15GENIChomozygous803073801
5139700094139700095CT13GENIChomozygous803073802
5139701742139701743TC29GENIChomozygous803073803
5139709936139709937CT22GENIChomozygous803073804
5139711213139711214GA19GENICpossibly homozygous803073805
5139717152139717153CT17GENICpossibly homozygous803073806
5139724327139724328TA15GENIChomozygous803073807
5139724858139724859CG7GENIChomozygous803073808
5139727912139727913TA20GENIChomozygous803073809
5139733451139733452AG21GENIChomozygous803073810
5139733937139733938AC13GENIChomozygous803073811
5139734191139734192TC12GENIChomozygous803073812
5139735976139735977AT15GENIChomozygous803073813
5139736164139736165CT15GENIChomozygous803073814