chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118894072118894073TG16GENIChomozygous116674816
8118894088118894089TA10GENIChomozygous116674818
8118894091118894092CT10GENIChomozygous116674820
8118894225118894226TG7GENIChomozygous116674822
8118894226118894227TC7GENIChomozygous116674824
8118894239118894240TC8GENIChomozygous117062295
8118894357118894358TG19GENIChomozygous117062297
8118894412118894413GC20GENIChomozygous117062299
8118894413118894414GA20GENIChomozygous117062301
8118894541118894542AG29GENIChomozygous117062303
8118894970118894971AG23GENIChomozygous117062305
8118895278118895279GA27GENIChomozygous117062307
8118895316118895317TC29GENIChomozygous117062309
8118895362118895363AG26GENICpossibly homozygous117062311
8118895441118895442GA31GENIChomozygous117062313
8118895556118895557AG36GENIChomozygous117062315
8118895655118895656CT38GENIChomozygous117062317
8118895742118895743AG38GENIChomozygous117062319
8118895928118895929TC24GENIChomozygous117062321
8118896060118896061TC15GENIChomozygous117062323
8118896105118896106CT17GENIChomozygous117062325
8118896603118896604TC34GENIChomozygous117062327
8118896686118896687GC25GENIChomozygous117062329
8118896892118896893AC21GENIChomozygous117062331
8118896928118896929GA28GENICpossibly homozygous117062333
8118897064118897065TG27GENIChomozygous117062335
8118899257118899258TC25GENIChomozygous116674848
8118910815118910816GA25GENIChomozygous117062337
8118918641118918642AG46GENIChomozygous116675109
8118922780118922781AG24GENIChomozygous116675175