chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13103523118103523119CT37GENIChomozygous49872694
13103524788103524789A-30GENICpossibly homozygous49872697
13103525420103525421TC21GENIChomozygous49872698
13103525975103525976GA19GENIChomozygous49872699
13103526655103526656TC27GENIChomozygous49872700
13103527462103527463AG16GENIChomozygous49872701
13103527487103527490AAA---4GENICheterozygous49872702
13103527981103527982CT13GENIChomozygous49872703
13103528280103528281AG13GENIChomozygous49872706
13103529659103529660GGT24GENIChomozygous49872707
13103529761103529762AG24GENIChomozygous49872708
13103530308103530309TTC26GENIChomozygous49872709
13103530795103530796TC25GENIChomozygous49872710
13103531404103531405TC16GENIChomozygous49872712
13103531460103531461G-10GENIChomozygous49872713
13103531595103531596AG19GENIChomozygous49872714
13103532369103532370CCG20GENIChomozygous49872715
13103532980103532981AG18GENIChomozygous49872716
13103525457103525464TTTTTTT-------6GENICheterozygous50620281
13103533084103533085GGCACA8GENICpossibly homozygous50620282
13103533129103533131CT--2GENIChomozygous50620283
13103533180103533181TTCACACACACACA3GENIChomozygous50620284
13103535663103535664TC33GENIChomozygous49872717
13103537529103537530TC39GENIChomozygous49872721
13103537599103537600GC34GENIChomozygous49872722
13103539836103539837TC19GENIChomozygous49872723
13103539838103539839TC20GENIChomozygous49872724
13103536126103536130TGTG----23GENIChomozygous50597272
13103536076103536077T-12GENICheterozygous50620285
13103536078103536079T-12GENICheterozygous50620286
13103540451103540452GGT20GENICheterozygous49872725
13103540783103540784AG8GENIChomozygous49872726
13103541194103541195TC30GENIChomozygous49872727
13103541789103541790TC25GENIChomozygous49872728
13103542792103542793GGGAAAA18GENIChomozygous50620288
13103543932103543934CA--17GENICpossibly homozygous49872729
13103545731103545732CT34GENIChomozygous49872730
13103539988103539989TTACACACACACACACACAC5GENIChomozygous50566613