chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141617983141617984AG25GENIChomozygous54159368
7141618022141618023GT34GENICpossibly homozygous54267326
7141618025141618026TTTTTG27GENIChomozygous54159369
7141618438141618439TTGG1GENIChomozygous54159370
7141618447141618448GGGGGAC2GENIChomozygous54267329
7141620382141620384AG--39GENIChomozygous54159371
7141620684141620685AAG20GENIChomozygous54159372
7141620803141620804AG35GENIChomozygous54159373
7141621272141621273TTAC13GENICpossibly homozygous54159374
7141622263141622264AAT30GENICheterozygous54267331
7141622762141622763CCT20GENICpossibly homozygous54159377
7141623224141623225GT42GENIChomozygous54159378
7141623244141623245CT43GENIChomozygous54267335
7141623958141623959GA29GENIChomozygous54159379
7141624365141624366AG18GENIChomozygous54159381
7141624432141624433GGGGGGCC1GENIChomozygous54267338
7141625703141625704GA38GENIChomozygous54159382
7141625877141625889AAAAAAAAAAAA------------4GENICheterozygous54267341
7141626304141626305GA33GENIChomozygous54159383
7141626534141626535AG23GENIChomozygous54267344
7141626564141626565GGAA14GENIChomozygous54159384
7141626607141626608GA27GENIChomozygous54267347
7141626840141626841AG36GENIChomozygous54159386
7141627008141627009AG26GENICheterozygous54678534
7141627012141627013AG27GENICheterozygous54267350
7141627024141627025GA30GENICheterozygous54159391
7141627028141627029GA32GENICheterozygous54159392
7141627085141627086G-31GENIChomozygous54267353
7141627218141627219TC31GENIChomozygous54159395
7141627497141627498CCAATAGTCGAGTCTGTTA11GENIChomozygous54159397
7141627970141627971GA39GENIChomozygous54159398
7141629205141629206CT32GENICheterozygous54529692
7141632965141632966CCA15GENICheterozygous54159406
7141633159141633160CCAA10GENICheterozygous54159407
7141633376141633377CCAAA7GENICpossibly homozygous54267355
7141633390141633391C-27GENIChomozygous54159408
7141633549141633550CT35GENIChomozygous54267358
7141633953141633954GA34GENIChomozygous54267361