chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101509999715099998CT8GENICheterozygous116497711
101510000115100002CT10GENICheterozygous116497713
101510030615100307CT17GENICheterozygous116737568
101510057315100574TC19GENICheterozygous116497721
101510102115101022CT5GENIChomozygous116737569
101510205015102051GA19GENICheterozygous116497733
101510210215102103CT16GENICheterozygous116497735
101510212015102121CA15GENICheterozygous116497737
101510214415102145AG16GENICheterozygous116497739
101510214915102150CT16GENICheterozygous116497741
101510215015102151AG15GENICheterozygous116497743
101510216215102163CT19GENICheterozygous116497745
101510221215102213AG16GENICheterozygous116497747
101510225115102252AG16GENICheterozygous116497749
101510227315102274AG14GENICheterozygous116497751
101510230115102302AG14GENICheterozygous116497753