chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123445427334454274GA17GENIChomozygous139134725
123445484134454842AG16GENIChomozygous139134726
123445498934454990TC16GENIChomozygous139134727
123445534134455342AG26GENIChomozygous139134728
123445551534455516TA21GENIChomozygous139134729
123445566334455664GA17GENIChomozygous139134730
123445687934456880CT21GENIChomozygous139134731
123445716834457169AG11GENIChomozygous139134732
123445757934457583ACAC1GENIChomozygous147696544
123445794934457950A20GENICheterozygous403325612
123445794834457949CA20GENIChomozygous403325609
123445794834457949C20GENICheterozygous403325610
123445794934457950AC20GENIChomozygous403325611
123445824534458246CT21GENIChomozygous139134733
123445889434459009GTAATTTGAGTTTTCTTTTTTTTTTTGGTTCTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGTTCTACCACTGAGCTAAATCCCCAACCCCC15GENIChomozygous139053466
123445955234459553CA21GENIChomozygous139134734
123446106834461068G13GENIChomozygous139053467
123446150434461505GA15GENIChomozygous139134735
123446186234461880GAGGGGGCAGAGGAGGAG7GENIChomozygous139053468
123446325134463252CT19GENIChomozygous139134736
123446326234463262G14GENIChomozygous139053469
123446343534463436TA17GENIChomozygous139134737
123446369334463694GT17GENIChomozygous139134738
123446402434464024C7GENICpossibly homozygous139053470
123446441934464420TC14GENIChomozygous139134739
123446442134464422CA14GENIChomozygous139134740
123446442734464428TC12GENIChomozygous139134741
123446496134464962GA28GENIChomozygous139134742
123446511434465114CCTGATC15GENIChomozygous139053471
123446651434466514CAAA19GENIChomozygous139053472
123446667334466674AC24GENIChomozygous139134743