chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153661163236611636ATAG35GENIChomozygous129246012
153661342736613428CG7GENICheterozygous118913581
153661343236613433GA8GENICheterozygous118913583
153661346336613464CG17GENICheterozygous118913585
153661346836613469GA18GENICheterozygous118955716
153661348736613489CA17GENICheterozygous131519603
153662546336625464G13GENIChomozygous129246013
153662546536625466GT13GENIChomozygous124064096
153662547236625474CC14GENIChomozygous129246014
153662993236629933AT19GENICpossibly homozygous118913604
153663000436630005CT7GENICheterozygous118913606
153663002936630030GA4GENICheterozygous118999523
153663008136630082TG4GENICheterozygous129314763
153663046036630461A21GENICheterozygous133976506
153663047536630476TC20GENICheterozygous133977509
153663066036630661GA5GENICheterozygous133977510
153663077636630777CT9GENICheterozygous129314767
153663079236630793GA9GENICheterozygous129314768
153663187836631879CT14GENICheterozygous129314771
153663299136632992CT6GENICheterozygous131741860
153668158136681582TA13GENICheterozygous129314775
153670318536703186T16GENIChomozygous129246016
153670319636703199TAC13GENIChomozygous129246017
153671389136713892C27GENIChomozygous129246018
153671849536718495CAAAGGGTGTATTTTTCCCT15GENIChomozygous129246019
153671850136718502A9GENIChomozygous129246020
153671850336718504AC9GENIChomozygous124064166
153672783336727835AT26GENICheterozygous130148984
153673579536735795GG8GENIChomozygous129246021
153673580536735805GT10GENIChomozygous129246022
153673582836735829C20GENIChomozygous129246023