chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3117573819117573820CT17GENICheterozygous58389664
3117573950117573951AG13GENICheterozygous57620678
3117576266117576267GA17GENICheterozygous57620680
3117577545117577546CCAAAT13GENICheterozygous58178653
3117577728117577729AG15GENICheterozygous58389667
3117578439117578440A-10GENICheterozygous58389668
3117579216117579217GT16GENICheterozygous57620694
3117579569117579581ACACACACACAC------------6GENICheterozygous59046185
3117580192117580193CT26GENIChomozygous57620698
3117580253117580254TA22GENICheterozygous58389669
3117580513117580514GA11GENICheterozygous57620700
3117581122117581123CA11GENICheterozygous58389670
3117582128117582131TAA---8GENIChomozygous57620706
3117582948117582949CT19GENICheterozygous57620708
3117583062117583063TC22GENIChomozygous57620710
3117583416117583417GA18GENICheterozygous58389671
3117583538117583539CT18GENICheterozygous58389672
3117583720117583721CT12GENICheterozygous58389673
3117584120117584124TTTT----12GENICheterozygous57620714
3117584542117584543CT20GENICheterozygous58389674
3117585367117585368TC23GENICheterozygous57620722
3117585415117585416TC22GENIChomozygous57620724
3117585925117585926GA19GENICheterozygous57620726
3117585937117585938GA20GENICheterozygous57620728
3117586314117586315TC20GENIChomozygous57620730
3117586603117586604CT12GENICheterozygous57620732
3117586856117586857AT27GENIChomozygous57620734
3117587290117587291GA14GENICheterozygous57620738