chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9112580467112580468CT10GENICheterozygous52113572
9112599700112599701AATG9GENICpossibly homozygous52113796
9112599744112599754TGTATGTGTG----------18GENICheterozygous52300427
9112604247112604248TC20GENICheterozygous52113836
9112615939112615997GCCCTCCAGGGCTCGCCCTCACTCCCATTGCCCTCCAGGGCTCACCCTCAGGACCATT----------------------------------------------------------13GENICheterozygous52868826
9112632965112632966GA10GENICheterozygous52300567
9112679601112679602GC7GENICheterozygous52114262
9112681341112681342AATG2GENIChomozygous52114278
9112702131112702132CCA8GENICheterozygous52114460
9112711357112711358GC13GENICheterozygous52114556
9112722869112722870TTAAA2GENICheterozygous52301092
9112735938112735939CT12GENICheterozygous52301131
9112751335112751336TTCC5GENICheterozygous52301167