chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2252931708252931709AG34GENIChomozygous74965722
2252932354252932355AT66GENICpossibly homozygous74965724
2252934482252934483CA53GENICheterozygous74965726
2252934813252934814GC56GENICheterozygous74965727
2252934843252934844CG50GENICheterozygous75104073
2252938536252938537TG35GENIChomozygous74965729
2252938752252938753TG30GENIChomozygous74965731
2252940761252940762GA65GENIChomozygous74965733
2252940779252940780GC61GENICpossibly homozygous74965735
2252941180252941181GA69GENIChomozygous74965737
2252941864252941865TA54GENIChomozygous74551239
2252944006252944007CA31GENIChomozygous74965739
2252945927252945928AT41GENIChomozygous74965741
2252946571252946572TC39GENIChomozygous74965743
2252947003252947004TC56GENIChomozygous74965745
2252947029252947030CG62GENIChomozygous74965746
2252947119252947120TC45GENIChomozygous74965748
2252947217252947218GA58GENIChomozygous74965750
2252947229252947230GA56GENIChomozygous74965752
2252947474252947475TC44GENIChomozygous74965754
2252947831252947832TG47GENIChomozygous74965756
2252947864252947865AC45GENIChomozygous74965758
2252948147252948148GA51GENIChomozygous74965760