chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3129652598129652599TC30GENIChomozygous617977222
3129652599129652600GA30GENIChomozygous617977223
3129653298129653299GA25GENIChomozygous617977224
3129653987129653988CT15GENIChomozygous617977225
3129654504129654505TTGTATGTTTCTC19GENIChomozygous742080986
3129654838129654839GA18GENIChomozygous617977226
3129656308129656325CAGGTCCCCCGGAAAGG-----------------27GENIChomozygous742080987
3129656985129656986GA25GENIChomozygous617977227
3129657111129657112CT27GENIChomozygous617977228
3129657568129657569GGA5GENICheterozygous742080988
3129657568129657569GGAA5GENICheterozygous742080989
3129658097129658098AAT22GENIChomozygous742080990
3129658262129658263CCTT9GENICpossibly homozygous742080992
3129659438129659439CT11GENIChomozygous617977229
3129659588129659589GC26GENIChomozygous617977230
3129660226129660227T-12GENIChomozygous742080993
3129661042129661043CT14GENIChomozygous617977231
3129663140129663141GA15GENIChomozygous617977232
3129664167129664168GGA8GENIChomozygous742080994
3129665319129665320AAT7GENIChomozygous742080995
3129665568129665569CG9GENIChomozygous617977233
3129666506129666507AT24GENIChomozygous617977234
3129667397129667407TTTTTTTTTT----------6GENICheterozygous742080996
3129668229129668230CT14GENIChomozygous617977235
3129668628129668629A-15GENIChomozygous742080997
3129668632129668633AC15GENIChomozygous617977236
3129669216129669217GA17GENIChomozygous617977237
3129669784129669785CT11GENIChomozygous617977238