chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4116927114116927115AG52GENIChomozygous71110275
4116927954116927955GA43GENIChomozygous72483659
4116928446116928447GT15GENIChomozygous71110318
4116928792116928793CT22GENIChomozygous71110329
4116930352116930353AG73GENIChomozygous71110333
4116931274116931275AC26GENIChomozygous72483661
4116932615116932616CT39GENIChomozygous72483663
4116933820116933821GA47GENIChomozygous72483665
4116934745116934746TC28GENIChomozygous71110337
4116934928116934929CT101GENICpossibly homozygous72483667
4116939792116939793GA23GENIChomozygous71110353
4116943194116943195GA52GENIChomozygous71110361
4116956364116956365CG12GENIChomozygous71110445
4116965066116965067GT16GENIChomozygous72483669
4116967204116967205CG52GENICheterozygous72711361