chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77051600970516010GA48GENIChomozygous53956710
77051766170517662AT37GENIChomozygous53956712
77051856870518569TC57INTERGENIChomozygous53956714
77051948470519485CT9INTERGENIChomozygous53956716
77051952570519526GC5INTERGENICheterozygous53956717
77051952770519528AAG3INTERGENIChomozygous53956719
77051999270519993TC44INTERGENIChomozygous53956721
77052048170520482AAT32INTERGENIChomozygous53956723
77052065470520657ACA---18INTERGENICheterozygous53956725
77052065670520659ACA---18INTERGENIChomozygous53956727
77052181370521814AG35GENIChomozygous53956729
77052260870522609GT50GENIChomozygous53956731
77052292070522924CTAA----48GENIChomozygous53956733
77052730570527306GC68GENIChomozygous53956735
77052886870528869CCT31GENICheterozygous53956737
77052888170528882TTC37GENICheterozygous53956739
77053459470534595AAAT36GENIChomozygous53956741
77053583970535840GT30GENIChomozygous53956743
77053708670537087AAG30GENIChomozygous53956745
77053709170537092CCTGATATGGA30GENIChomozygous53956747
77053882670538827AAACAC8GENICheterozygous53956749
77053937270539376AAAC----18GENIChomozygous53956751
77054078970540790AAC50GENIChomozygous53956753
77054085170540852C-25GENIChomozygous53956755
77054086070540861CCA29GENIChomozygous53956757
77054185870541859TTC3GENICheterozygous53956759
77054411070544111GC37GENIChomozygous53956761
77054730470547305AAAC39GENICpossibly homozygous53956763
77055062270550623TC45GENIChomozygous53956765
77055104770551048GA55GENIChomozygous53956767
77055258570552586GA51GENIChomozygous53956769