chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4160735125160735129TGTG----9GENIChomozygous58482522
4160737395160737396TTTCAC33GENIChomozygous57540573
4160739729160739731GT--25GENIChomozygous57540575
4160741034160741054GGTTAGGGATTTAGCTCAGT--------------------23GENIChomozygous57540577
4160741118160741119CCA8GENICheterozygous57003247
4160745299160745300AG31GENIChomozygous57540581
4160746495160746496AG28GENIChomozygous57540583
4160747094160747095GGC17GENIChomozygous57540585
4160747151160747152AC17GENIChomozygous57540587
4160748311160748312TA31GENIChomozygous57540589
4160748489160748490GT16GENIChomozygous57540591
4160749265160749274GAAACAAAC---------9GENICheterozygous58350507
4160749273160749274CCA8GENICheterozygous57003248
4160749335160749336GA6GENIChomozygous57540597
4160749863160749864AC25GENIChomozygous57540599
4160749970160749971GA20GENIChomozygous58482524
4160749971160749972AC20GENIChomozygous57844143
4160752684160752685CCACACAG7GENICheterozygous58482526
4160752684160752685CCACACACAG7GENICheterozygous58482528
4160753419160753420AG25GENIChomozygous57540605
4160753820160753821T-8GENICheterozygous57540607
4160754008160754012GCAG----16GENICheterozygous58350513
4160754762160754763CA21GENIChomozygous57540609
4160756881160756882CCT23GENIChomozygous57540611
4160758201160758202AAACAC6GENIChomozygous57540615