chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2252931708252931709AG16GENIChomozygous74965722
2252932354252932355AT31GENIChomozygous74965724
2252938752252938753TG28GENIChomozygous74965731
2252940761252940762GA20GENIChomozygous74965733
2252940779252940780GC23GENIChomozygous74965735
2252941180252941181GA15GENIChomozygous74965737
2252945927252945928AT51GENIChomozygous74965741
2252946571252946572TC21GENICpossibly homozygous74965743
2252947003252947004TC35GENIChomozygous74965745
2252947029252947030CG37GENIChomozygous74965746
2252947119252947120TC29GENIChomozygous74965748
2252947217252947218GA28GENIChomozygous74965750
2252947229252947230GA32GENIChomozygous74965752
2252947474252947475TC53GENIChomozygous74965754
2252947831252947832TG42GENIChomozygous74965756
2252947864252947865AC46GENIChomozygous74965758
2252948147252948148GA31GENIChomozygous74965760