Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:103372453-103372542 | Rare:16 | ||||
chr8:103414578-103414742 | Common:5; Rare:53 | ||||
chr8:103414831-103414879 | Rare:12 | ||||
chr8:103415013-103415482 | Common:6; Rare:241 | ||||
chr8:106270011-106270356 | Common:1; Rare:130 | ||||
chr8:106657557-106657924 | Common:5; Rare:104 | ||||
chr8:108248654-108248872 | Rare:89 | ||||
chr8:108443437-108443660 | Common:4; Rare:97 | ||||
chr8:109334016-109334406 | Common:1; Rare:113 | ||||
chr8:116873976-116874127 | Common:1; Rare:38 | ||||
chr8:116874170-116874197 | Rare:7 | ||||
chr8:116874201-116874253 | Rare:17 | ||||
chr8:116874611-116874935 | Common:6; Rare:136; Clinvar (benign):1 | ||||
chr8:116938408-116938509 | Common:4; Rare:40 | ||||
chr8:117520527-117520808 | Common:5; Rare:70 |