chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72312055923120560GT20GENIChomozygous146449285
72312077523120776TA21GENIChomozygous138034895
72312121223121213AG18GENIChomozygous138034896
72312279423122795CT17GENIChomozygous154436523
72312279423122795C17GENICheterozygous403204353
72312427423124275AT17GENIChomozygous138034904
72312538723125388CT27GENIChomozygous148020003
72312595323125954TC27GENIChomozygous138034913
72312671423126715CT19GENIChomozygous146449286
72312751023127511GT20GENIChomozygous138034917
72312775223127754TT16GENIChomozygous137941595
72312680823126808C23GENIChomozygous137941591
72312737323127373T32GENIChomozygous137941592
72312737523127375TTGCGGGCA32GENIChomozygous137941593
72312796223127963CT27GENIChomozygous138034919
72312824823128256CTAGGCTA29GENIChomozygous146435755
72312870623128707CT14GENIChomozygous146449287
72312920823129208A16GENIChomozygous146435756
72313025423130255CT15GENIChomozygous138034932
72313066523130666TG27GENIChomozygous138034935