chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104289364942893650TC28GENIChomozygous116576996
104289445242894453CA14GENIChomozygous117178042
104289594342895944TC37GENIChomozygous116576998
104289604242896043TG22GENIChomozygous117007536
104289977142899772GT20GENIChomozygous117252145
104290008442900085AG32GENIChomozygous116577006
104290050542900506AG22GENIChomozygous116577008
104290090642900907AG27GENIChomozygous116577010
104290207642902077AG27GENIChomozygous116577014
104290218542902186AC38GENIChomozygous116577016
104290236842902369CA29GENIChomozygous116577018
104290474742904748CA35GENIChomozygous116577020
104290487942904880GC4GENIChomozygous116577026
104290488742904888GA3GENIChomozygous116577028
104291617842916179CG40GENIChomozygous117252147
104291692042916921AC28GENIChomozygous116577030
104291937042919371CT18GENIChomozygous117007538
104292048142920482TC28GENIChomozygous117007539
104292114342921144AG23GENIChomozygous116577036
104290488842904889TG3GENIChomozygous116765908
104292445242924453AG23GENIChomozygous116577038
104292826242928263TC14GENIChomozygous117007540
104292938742929388GA17GENICheterozygous117077348
104292939142929392GA17GENICheterozygous117077349
104292990242929903TC20GENIChomozygous116577048
104293080742930808AG18GENIChomozygous116577050
104293131142931312TC39GENIChomozygous116577054
104293140042931401CT32GENIChomozygous117007541
104293141042931411CT31GENIChomozygous117007542
104293183442931835AG27GENIChomozygous116577056
104293224542932246GA28GENIChomozygous117007543
104293229142932292AG32GENIChomozygous117007544