chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3131286892131286893GT14GENIChomozygous136822368
3131287584131287585GA19GENIChomozygous136822369
3131288154131288155AG19GENIChomozygous136822370
3131289539131289540GA18GENIChomozygous136822372
3131289833131289834TC6GENIChomozygous136822373
3131289858131289859AG6GENIChomozygous136822374
3131290010131290011TC7GENIChomozygous136822375
3131291560131291561GA16GENIChomozygous136822376
3131292237131292238AG19GENIChomozygous136822377
3131292998131292999GA21GENIChomozygous136822378
3131296796131296797CT14GENIChomozygous136822379
3131298753131298755GG1GENIChomozygous136591031
3131298759131298759TTTTCTAGTTCTTACTTCACTACTTC1GENIChomozygous136591032
3131298761131298761CAAT4GENIChomozygous136591033
3131298765131298766G5GENIChomozygous136591034
3131298771131298771T6GENIChomozygous136591035
3131298775131298780AACCG6GENIChomozygous136591036
3131298783131298783TA6GENIChomozygous136591037
3131298785131298786CG7GENIChomozygous136822380
3131298786131298787CG7GENIChomozygous136822381
3131298789131298790C7GENIChomozygous136591038
3131298791131298795CTCC9GENIChomozygous136591039
3131298796131298798GC10GENIChomozygous136591040
3131298798131298799CA10GENIChomozygous136822382
3131300596131300597AG13GENIChomozygous136822383
3131301016131301017TC11GENIChomozygous136822384
3131301850131301851GA20GENIChomozygous136822385
3131302222131302223CT32GENIChomozygous136822386
3131302504131302505A13GENIChomozygous136591041
3131302849131302850GA12GENIChomozygous154142203
3131302851131302852GA12GENIChomozygous136822387
3131303321131303322CT11GENIChomozygous136822388
3131307832131307833TC15GENIChomozygous136822389
3131308941131308942GA9GENIChomozygous136822390
3131309074131309075TG17GENIChomozygous136822391
3131309092131309093GA22GENIChomozygous136822392
3131309830131309830TA14GENIChomozygous136591042
3131309968131309969CT15GENIChomozygous136822393
3131311277131311278GT11GENIChomozygous136822394
3131302849131302850G12GENICheterozygous403713156