chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3149382373149382374TC44GENIChomozygous111772204
3149382614149382615GC40GENIChomozygous111772206
3149384015149384016TC34GENICpossibly homozygous111772208
3149384789149384790CT29GENIChomozygous111772210
3149384795149384796AG28GENIChomozygous111772212
3149385372149385373TC3GENIChomozygous111772214
3149385376149385377TC8GENIChomozygous111772216
3149385451149385452CT22GENIChomozygous111772218
3149385864149385865CT21GENIChomozygous111772220
3149387268149387269GA30GENIChomozygous111772222
3149388883149388884GA30GENIChomozygous111772224
3149388909149388910AG37GENIChomozygous111772226
3149390713149390714GT31GENIChomozygous111772228
3149390868149390869TG38GENIChomozygous111772230
3149391316149391317TA43GENIChomozygous111772232
3149391588149391589GA27GENIChomozygous111772234
3149391914149391915CA56GENIChomozygous111772236
3149392638149392639TC31GENIChomozygous111772238
3149392877149392878TC30GENIChomozygous111772240
3149393287149393288TG30GENIChomozygous111772242
3149393497149393498GA40GENIChomozygous111772244
3149393525149393526AC43GENIChomozygous111772246
3149393717149393718AG34GENIChomozygous111772248