chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3148082794148082795CT17GENIChomozygous111768436
3148083469148083470GC13GENIChomozygous111768438
3148083716148083717CT13GENIChomozygous112186635
3148084473148084474CT20GENIChomozygous111768440
3148085049148085050AT24GENIChomozygous111768442
3148085065148085066AG26GENIChomozygous111768444
3148085891148085892TC21GENIChomozygous111768446
3148086426148086427AG15GENIChomozygous111768448
3148086568148086569CT26GENIChomozygous111768450
3148086634148086635TC18GENIChomozygous111768452
3148086638148086639CT17GENIChomozygous111768454
3148086673148086674AG17GENIChomozygous111768456
3148086743148086744TC16GENIChomozygous111768458
3148087101148087102AG19GENIChomozygous111768460
3148087303148087304GA20GENICpossibly homozygous111768462
3148088021148088022CA1GENIChomozygous111768464
3148083790148083791TC25GENIChomozygous127994042
3148088214148088216CA9GENIChomozygous127940689
3148088739148088743TTTA26GENIChomozygous127940690
3148089549148089549C23GENIChomozygous127940691
3148089721148089722CT20GENIChomozygous111768466
3148089939148089940CG15GENIChomozygous127994043
3148090016148090017AC16GENIChomozygous111768468
3148090546148090547GA30GENIChomozygous111768470
3148090555148090556GA31GENIChomozygous111768472
3148090706148090707AC20GENIChomozygous111768474
3148090855148090896GAAGCAGGATTGGCTGAGGGACACCTAGGCATCTGTAAGCC13GENIChomozygous127940692
3148091089148091090TG30GENIChomozygous111768480