chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3129652598129652599TC13GENIChomozygous663014667
3129652599129652600GA13GENIChomozygous663014668
3129653298129653299GA32GENIChomozygous663014669
3129653987129653988CT20GENIChomozygous663014670
3129654504129654505TTGTATGTTTCTC20GENIChomozygous764896201
3129654838129654839GA29GENIChomozygous663014671
3129656308129656325CAGGTCCCCCGGAAAGG-----------------18GENIChomozygous764896202
3129656985129656986GA27GENIChomozygous663014672
3129657111129657112CT22GENIChomozygous663014673
3129657568129657569GGA6GENICheterozygous764896203
3129657568129657569GGAA6GENICheterozygous764896204
3129658097129658098AAT12GENIChomozygous764896205
3129658262129658263CCTT8GENICheterozygous764896207
3129659438129659439CT30GENIChomozygous663014674
3129659588129659589GC35GENIChomozygous663014675
3129660226129660227T-16GENICpossibly homozygous764896208
3129660358129660359CCA8GENICheterozygous764896209
3129661042129661043CT27GENIChomozygous663014676
3129663140129663141GA32GENIChomozygous663014677
3129664167129664168GGA14GENICpossibly homozygous764896210
3129665319129665320AAT10GENICpossibly homozygous764896211
3129665363129665364TTGTGCTTGCTAGGCAA3GENIChomozygous764896212
3129665366129665367GGCTCT2GENIChomozygous764896213
3129665367129665368AAC2GENIChomozygous764896214
3129665369129665370AACTGAGC2GENIChomozygous764896215
3129665568129665569CG21GENIChomozygous663014678
3129666506129666507AT26GENIChomozygous663014679
3129667397129667407TTTTTTTTTT----------5GENICheterozygous764896216
3129668229129668230CT21GENIChomozygous663014680
3129668628129668629A-19GENIChomozygous764896217
3129668632129668633AC20GENIChomozygous663014681
3129669216129669217GA32GENIChomozygous663014682
3129669784129669785CT29GENIChomozygous663014683