chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147744870147744871AG26GENICheterozygous113059390
4147744884147744885AG27GENICheterozygous113059392
4147744893147744894TG23GENICheterozygous113059394
4147744902147744903TG25GENICheterozygous113059396
4147745072147745073CT24GENIChomozygous112874961
4147745447147745448AG20GENIChomozygous112874962
4147746422147746423AG26GENIChomozygous112874964
4147746759147746760CT14GENIChomozygous112874965
4147746881147746882AC13GENIChomozygous112874966
4147747002147747003TC10GENIChomozygous112874967
4147747117147747118GA18GENIChomozygous112874968
4147747310147747311CT18GENIChomozygous112874969
4147748124147748125TC22GENIChomozygous112874970
4147748297147748298TC28GENIChomozygous112874971
4147749508147749509TC14GENIChomozygous112874972
4147749643147749644AG12GENIChomozygous112874973
4147749856147749857AG10GENIChomozygous112874974
4147750735147750736CG18GENIChomozygous112874975
4147751820147751821CT32GENIChomozygous112874976
4147752908147752909AG10GENIChomozygous112874977
4147754966147754967GA8GENIChomozygous112874980
4147756091147756092TC23GENIChomozygous112874981