chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134939767749397678TG36GENICheterozygous115067174
134943464549434646CT60GENIChomozygous114337996
134944100049441001CA136GENICheterozygous118450426
134944101549441016TC128GENICheterozygous118450427
134944105049441051GT98GENICheterozygous118450428
134945412349454124GC32GENICpossibly homozygous114337998
134945412549454126TC32GENIChomozygous114338000
134945413249454133CA32GENICpossibly homozygous114338002
134945413949454140TC36GENIChomozygous114338004
134947304049473041TG103GENICheterozygous118450429
134947310549473106GT233GENICheterozygous118450430
134947310649473107GC237GENICheterozygous118450431
134947310949473110AT249GENICheterozygous118450432
134947311349473114TG250GENICheterozygous118450433
134947319349473194TC248GENICheterozygous118450435
134947319749473198TA246GENICheterozygous118450436
134948081849480819GC248GENICheterozygous118498224
134948082449480825AT248GENICheterozygous118498225
134948084749480848GT246GENICheterozygous118498226
134945833549458336AG39GENICpossibly homozygous118591911
134947229649472297CA59GENICheterozygous118591912
134948187649481877AT83GENICheterozygous118591913