chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108918114089181141TTG1INTERGENIChomozygous51536739
108918114289181143CT2INTERGENIChomozygous52394366
108918303689183037GA4INTERGENIChomozygous51536742
108918367689183677TC11INTERGENICheterozygous51536743
108918417289184173TC5INTERGENIChomozygous51536744
108918632189186322AT10INTERGENIChomozygous51536746
108918878089188781CCG13INTERGENICpossibly homozygous51536761
108918990389189904CT5INTERGENIChomozygous51536762
108919071689190717AAT3INTERGENICheterozygous51536765
108919071789190718T-3INTERGENICheterozygous52574208
108919149789191498CT12INTERGENIChomozygous51536766
108919170289191703CT18INTERGENIChomozygous51536767
108919267689192677GA18GENICpossibly homozygous51536768
108919366689193667AG9GENICpossibly homozygous51536769
108919482789194828C-4GENIChomozygous51536770
108919508489195085AG14GENIChomozygous51536771
108919812789198128CT20GENIChomozygous51536773