chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25293560252935603A-24GENICheterozygous686970099
25293561352935617AAAT----25GENICheterozygous686970100
25293561552935617AT--27GENIChomozygous686970101
25293561652935617T-25GENIChomozygous686970102
25293589952935900TC20GENIChomozygous512272553
25293680452936805CG25GENIChomozygous512272554
25293756752937569AC--25GENIChomozygous686970103
25293888052938881T-17GENIChomozygous686970104
25293933752939338CT17GENIChomozygous512272555
25293978552939786TC24GENIChomozygous512272556
25294119252941193AG27GENIChomozygous512272557
25294410352944104AG27GENIChomozygous512272558
25294463052944631AG25GENIChomozygous512272559
25294583452945835CG18GENIChomozygous512272560
25294607052946071GGGTGTTTCA15GENIChomozygous686970105
25295003752950038TC29GENIChomozygous512272561
25295132552951326AT22GENIChomozygous513976001
25295178752951788A-18GENIChomozygous686970106
25295233852952339AG22GENIChomozygous512272562
25295588152955882TG33GENIChomozygous512272563
25295847652958477CCA7GENICpossibly homozygous686970107
25295851152958512A-12GENICpossibly homozygous686970109
25296030952960310AT23GENIChomozygous512272564
25296360052963601A-3GENIChomozygous686970111
25296390052963901T-7GENIChomozygous686970112
25296390252963911TTTGATATT---------5GENIChomozygous686970113
25296390952963911TT--1GENIChomozygous686970114
25296391652963918TG--8GENIChomozygous686970115
25296481852964821TTA---2GENIChomozygous686970117
25296539252965393TC20GENIChomozygous512272565
25296585352965854TTTTTTTTTTTTCATGAAACATG12GENIChomozygous686970119
25296595552965956CT24GENIChomozygous513976002
25296798152967982AG32GENIChomozygous512272566
25297017052970171AG11GENIChomozygous512272567