chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143500466143500467TC11GENIChomozygous114151489
5143508925143508925TCCCT17GENIChomozygous128249305
5143529815143529816CA19GENIChomozygous114035260
5143529847143529848CT19GENIChomozygous114344609
5143529851143529852CG19GENIChomozygous114035262
5143529871143529872CT16GENIChomozygous114344611
5143529708143529708GT25GENIChomozygous130315119
5143615977143615979TG32GENICheterozygous130315121
5143529817143529818T19GENIChomozygous130315120
5143616773143616774G46GENIChomozygous128249334
5143616794143616795AG46GENIChomozygous114035326
5143617138143617138T47GENIChomozygous128249335
5143617150143617150C50GENIChomozygous128249336
5143617174143617174T44GENIChomozygous128249337
5143617187143617187A45GENIChomozygous128249338
5143617193143617193T44GENIChomozygous128249339
5143620250143620250T30GENIChomozygous128249340
5143620264143620265T27GENIChomozygous128249341
5143620390143620391G41GENIChomozygous128249342
5143620412143620413A44GENIChomozygous128249343
5143665489143665491CA33GENICheterozygous130315122
5143681034143681035T18GENIChomozygous130315123
5143681088143681088T19GENIChomozygous128249359
5143692165143692165G39GENIChomozygous128249366
5143692175143692176AG34GENIChomozygous114035585
5143692186143692186G36GENIChomozygous128249368
5143692196143692196GT36GENIChomozygous128249369
5143692202143692203A35GENIChomozygous128249370
5143692218143692218G34GENIChomozygous128249371
5143692227143692228A33GENIChomozygous128249373
5143692252143692253A38GENIChomozygous128249374
5143692259143692260A41GENIChomozygous128249375