chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48120841381208414TC29GENIChomozygous112748239
48120950581209505AAAC23GENIChomozygous128054356
48120973081209731GA31GENIChomozygous113036419
48121313281213133AT29GENIChomozygous112748243
48121339981213400TC29GENIChomozygous112748245
48121580381215804GA16GENIChomozygous112748249
48121656381216564AG33GENIChomozygous112748251
48121831081218311T25GENICpossibly homozygous128054357
48121837181218372TA24GENIChomozygous112748253
48122000081220001AG25GENIChomozygous112748259
48121868381218684CT22GENIChomozygous113036421
48121920481219205TC28GENIChomozygous112748255
48122001381220014GA26GENIChomozygous112748261
48122124381221244GA37GENIChomozygous112748265
48122126181221262CT41GENIChomozygous112748267
48122146881221469CT24GENIChomozygous113036423
48122308881223088AC28GENIChomozygous128054359
48122392181223922AG31GENIChomozygous112748271
48122528381225284GA24GENIChomozygous112748275
48123060681230607GT33GENIChomozygous112748285
48122565681225657AC31GENIChomozygous112748277
48122687581226876TC39GENIChomozygous112748279