chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
193676688236766883CT27GENICpossibly homozygous46109418
193676713236767133CT12GENICpossibly homozygous46109420
193676758236767583AG7GENIChomozygous46109422
193676863636768637CCACACACACACACACACACACAT6GENICheterozygous46380045
193676948336769484GGA6GENICheterozygous46109434
193676954036769541CA3GENIChomozygous46380047
193676954136769542AC3GENIChomozygous46380049
193676955336769554AG9GENIChomozygous46109438
193676958336769584C-17GENIChomozygous46109440
193676961136769612TA14GENIChomozygous46109442
193676961536769616GGC12GENIChomozygous46109444
193677254036772541CCTA17GENIChomozygous46109445
193677622436776225TTCA3GENIChomozygous46109449
193677678636776787AC2GENIChomozygous46109451
193677374636773747A-4GENICheterozygous46429696