chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115708107457081075GA77GENICheterozygous138997456
115708108557081086AG79GENICheterozygous138997457
115708112357081124CA84GENICheterozygous138997458
115708112557081126GA85GENICheterozygous138997459
115708114557081146CT85GENICheterozygous138997460
115709535157095351AGG9GENIChomozygous138890605
115709545257095453GA19GENIChomozygous138997461
115709546157095462GA17GENIChomozygous138997462
115709547057095471GA16GENIChomozygous138997463
115709553057095531A7GENIChomozygous138890606
115709553557095536G6GENIChomozygous138890607
115709554557095547GT7GENIChomozygous138890608
115709555257095553GA7GENIChomozygous138997464
115709555257095553G7GENICheterozygous403774840
115709545257095453G19GENICheterozygous403306560
115709546157095462G17GENICheterozygous403306561
115709547057095471G16GENICheterozygous403306562
115710890957108910G36GENICheterozygous403306563
115718413157184132A32GENICheterozygous138890609
115718718357187183A53GENIChomozygous138890610
115721514157215142TC32GENICpossibly homozygous138997465
115736118757361189GT21GENICheterozygous138890611
115747244257472443A10GENICheterozygous404521910
115710890957108910GC36GENICheterozygous403306564
115714147457141475T5GENIChomozygous403774841
115714147457141475TC5GENICheterozygous403774842
115747244257472443AG10GENICheterozygous404521911
115757636257576363A24GENICheterozygous403306567
115757636257576363AG24GENICheterozygous403306568
115757636457576365A24GENICheterozygous403306569
115757636457576365AG24GENICheterozygous403306570
115760386257603863T21GENICheterozygous403306583
115760386257603863TA21GENICheterozygous403306584
115760622957606230A50GENICpossibly homozygous138890612
115764211757642118CT64GENIChomozygous138997466