Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:73322691-73322971 | Rare:63 | ||||
chr8:86451158-86451209 | Rare:5 | ||||
chr8:89748000-89748043 | Rare:7 | ||||
chr8:89935581-89935879 | Common:1; Rare:55; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr8:90004417-90004672 | Common:2; Rare:43 | ||||
chr8:90022765-90023058 | Common:1; Rare:54 | ||||
chr8:91068535-91068832 | Rare:58 | ||||
chr8:91069604-91069690 | Common:1; Rare:13 | ||||
chr8:93719958-93719976 | Rare:6 | ||||
chr8:94258350-94258556 | Common:1; Rare:34 | ||||
chr8:94766474-94766641 | Rare:35 | ||||
chr8:94866127-94866192 | Common:1; Rare:19 | ||||
chr8:96602195-96602426 | Common:1; Rare:46 | ||||
chr8:96965845-96965999 | Common:1; Rare:36 | ||||
chr8:97275612-97275915 | Common:2; Rare:60 |