chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2048922584892259AG81GENICheterozygous801143470
2048923034892304CT98GENICheterozygous801143471
2048923064892307CT99GENICheterozygous801143472
2048928324892833GA32GENICheterozygous801143473
2048928584892859CT57GENICheterozygous801143474
2048928764892877AG76GENICheterozygous801143475
2048928784892879TC78GENICheterozygous801143476
2048928894892890AG87GENICheterozygous801143477
2048928974892898TA92GENICheterozygous801143478
2048929024892903GA99GENICheterozygous801143479
2048929154892916CT89GENIChomozygous801143480
2048929304892931GC96GENICheterozygous801143481
2048929664892967TG149GENICheterozygous801143482
2048930074893008AG250GENICheterozygous801143483
2048930564893057CT250GENICheterozygous801143484
2048930574893058AT248GENICheterozygous801143485
2048930584893059TC250GENICheterozygous801143486
2048931064893107GA249GENICheterozygous801143487
2048931104893111CT249GENICheterozygous801143488
2048931624893163AG246GENICheterozygous801143489
2048931664893167AG243GENICheterozygous801143490
2048931684893169CT242GENICheterozygous801143491