chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101490301314903014GA21GENIChomozygous149633351
101490324514903246A21GENIChomozygous149631729
101490373014903731GA14GENIChomozygous149633352
101490536214905363CT19GENIChomozygous149633353
101490763714907638AG22GENIChomozygous142219157
101491023714910238TC21GENIChomozygous149633354
101491189614911897AG13GENIChomozygous142219161
101491279114912794TTG9GENIChomozygous149631730
101491288914912890CT13GENIChomozygous149633355
101491289614912897AC14GENIChomozygous142219163
101491428014914280AAAG19GENIChomozygous149631731
101491480314914804AG25GENIChomozygous142219165
101491292314912924CT19GENIChomozygous142219164
101491475114914752AT23GENIChomozygous149633356
101490697914906979GAAA16GENIChomozygous142197040
101491330714913307TCAC20GENIChomozygous142197043
101491683414916835CG17GENIChomozygous142219166
101491766114917661A15GENIChomozygous149631732
101491813414918135CT24GENIChomozygous149633357
101491876914918770TA32GENIChomozygous149633358
101491920914919210GA31GENIChomozygous149633359
101492109814921099GA15GENIChomozygous149633360
101492183614921836T18GENIChomozygous142197045
101492210914922109G25GENIChomozygous149631733
101492312614923127AT17GENIChomozygous149633361
101492312914923130AT17GENIChomozygous142219171
101492319414923195GA11GENIChomozygous149633362
101492419714924198T22GENIChomozygous142197046
101492442714924428TC27GENIChomozygous142219172
101492618114926182A19GENIChomozygous144853675
101492622614926227CT17GENIChomozygous149633363
101492727514927276GA23GENIChomozygous149633364
101492798214927983GT15GENIChomozygous144859562
101492959814929599TC22GENIChomozygous142219174
101493183914931839AC17GENIChomozygous144853676
101493262414932625CT30GENIChomozygous142219175
101493477014934771GA19GENIChomozygous149633365
101490871814908719GA12GENIChomozygous404969735
101490875514908756A12GENICheterozygous403277080
101490875514908756AG12GENIChomozygous403277081