chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117574602117574603GA34GENIChomozygous116672000
8117574873117574874CT45GENICpossibly homozygous116988178
8117575608117575609GA43GENIChomozygous116672002
8117576152117576153CT33GENIChomozygous116672004
8117579060117579061TC48GENIChomozygous116988179
8117579086117579087TC43GENIChomozygous116672006
8117580189117580190AC58GENICpossibly homozygous116672008
8117580267117580268GA44GENIChomozygous116672010
8117581875117581876TC51GENIChomozygous116672012
8117582166117582167CT54GENIChomozygous116672014
8117584809117584810AT31GENICpossibly homozygous116672016
8117590581117590582TG54GENICpossibly homozygous116672018
8117593787117593788GA25GENICheterozygous116672020
8117596942117596943AC44GENIChomozygous116672022
8117597287117597288CA24GENICheterozygous116672024
8117597825117597826AG50GENIChomozygous116672026
8117599006117599007AG63GENIChomozygous116672028
8117599030117599031AG57GENIChomozygous116672030