chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106850662968506630TA11GENIChomozygous126385443
106850669568506696TG15GENIChomozygous126385444
106850677668506777CA5GENIChomozygous116622263
106853338868533389CA5GENICheterozygous126422649
106853705868537059GA5GENIChomozygous116622344
106853706368537064AT6GENIChomozygous116622346
106853708668537087GT10GENIChomozygous116622348
106853712568537126GT18GENIChomozygous116622350
106853718068537181TG9GENIChomozygous116622352
106854765768547658AG21GENIChomozygous116622380
106854977668549777CG12GENIChomozygous126385447
106856324468563245GT10GENICheterozygous126385448
106857021068570211GA17GENIChomozygous126385451
106874980268749803CG3GENICheterozygous126461223
106875116968751170CA17GENIChomozygous126385459
106878199168781992TA3GENICheterozygous126461224
106879297368792974AG18GENIChomozygous126385463
106883557168835572GT10GENIChomozygous126385470
106883559468835595CT8GENIChomozygous126432806
106884900168849002CT10GENIChomozygous126385472
106890806668908067TG13GENIChomozygous126442315
106891461568914616GT13GENIChomozygous126385478
106905198069051981TA4GENICheterozygous126432824
106934345469343455GC10GENIChomozygous126385530
106934347369343474CG6GENIChomozygous126385531
106934347469343475CT6GENIChomozygous126385532
106934350969343510CG11GENIChomozygous126385533