chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121513392915133930TTCCCC13GENICheterozygous732032180
121513393115133932AC13GENICheterozygous608658467
121513415715134158TTAA20GENIChomozygous732032182
121513429815134299TTC22GENICpossibly homozygous732032185
121513451415134515T-7GENICpossibly homozygous732032186
121513479115134792AG22GENIChomozygous607559531
121513544815135449GT15GENIChomozygous608658468
121513550615135507T-11GENIChomozygous732032187
121513566115135662GA16GENIChomozygous607559532
121513590415135905TA17GENIChomozygous607559533
121513759615137597AAACACACACAC4GENICheterozygous732032189
121513759615137597AAACACACACACAC4GENICheterozygous732032190
121513831815138319CCCTGTCTGTCTGT14GENIChomozygous732032192
121513841615138417CCGTGT6GENICheterozygous732032193
121513841615138417CCGTGTGT6GENICheterozygous732032194
121513841615138417CCGTGTGTGT6GENICheterozygous732032195
121513945615139458TT--16GENICheterozygous732032196
121513945715139458T-16GENICheterozygous732032197
121513984915139850GA16GENIChomozygous607559534
121514078615140787TTC17GENIChomozygous732032199
121514135915141360GC26GENIChomozygous607559535
121514279915142800TC23GENIChomozygous608658469
121514562215145623TC17GENIChomozygous607559536
121514614915146150TTGCTCA20GENIChomozygous732032200
121514682515146826CT19GENIChomozygous607559537
121514699315146994AT42GENIChomozygous607559538
121514743015147431GA22GENIChomozygous607559539
121514824415148245CCATGTATGTATGTATGT17GENIChomozygous732032202
121514844315148444GGT16GENIChomozygous732032203
121514849715148498CT15GENIChomozygous607559540
121514871415148715TG21GENIChomozygous608658470
121514885615148857CG17GENIChomozygous608658471
121514940715149408AACTGGAACTCAAAGTTTACC30GENIChomozygous732032204
121515033115150332CT24GENIChomozygous607559541
121515078915150790CT30GENIChomozygous608658472
121515236015152361CT20GENIChomozygous607559542
121515246515152466GA19GENIChomozygous607559543