chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48120841381208414TC15GENIChomozygous112748239
48120950581209505AAAC14GENIChomozygous128054356
48121313281213133AT24GENIChomozygous112748243
48121339981213400TC22GENIChomozygous112748245
48121580381215804GA14GENIChomozygous112748249
48121656381216564AG29GENIChomozygous112748251
48121831081218311T17GENIChomozygous128054357
48121837181218372TA22GENIChomozygous112748253
48121913981219139C10GENIChomozygous128054358
48121920481219205TC20GENIChomozygous112748255
48122000081220001AG24GENIChomozygous112748259
48122001381220014GA24GENIChomozygous112748261
48122124381221244GA21GENIChomozygous112748265
48122126181221262CT22GENIChomozygous112748267
48122308881223088AC33GENIChomozygous128054359
48122392181223922AG27GENIChomozygous112748271
48122528381225284GA15GENIChomozygous112748275
48121148581211486GA15GENIChomozygous132837866
48121580181215802G13GENICheterozygous129902863
48121461881214619TC19GENIChomozygous119434796
48122529281225293AT16GENIChomozygous119434797
48122565681225657AC16GENIChomozygous112748277
48122687581226876TC23GENIChomozygous112748279
48123060681230607GT26GENIChomozygous112748285
48123146381231463C6GENIChomozygous128054361
48122918281229182A24GENIChomozygous132832580