| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:92965450-92965773 | Common:4; Rare:145 | ||||
| chr8:92966031-92966214 | Rare:65 | ||||
| chr8:93700426-93700648 | Common:2; Rare:176 | ||||
| chr8:93739990-93740580 | Common:1; Rare:254 | ||||
| chr8:93740768-93741205 | Common:1; Rare:184 | ||||
| chr8:93916620-93916970 | Common:9; Rare:208; Clinvar (benign):2 | ||||
| chr8:94475010-94475201 | Common:7; Rare:98 | ||||
| chr8:94553425-94553766 | Common:6; Rare:236 | ||||
| chr8:94719749-94719992 | Common:2; Rare:140 | ||||
| chr8:94895194-94895359 | Rare:94 | ||||
| chr8:94895651-94895851 | Common:3; Rare:109 | ||||
| chr8:94949308-94949625 | Common:6; Rare:168 | ||||
| chr8:95024738-95025135 | Common:4; Rare:258; Clinvar:2; Clinvar (benign):16; Clinvar (pathogenic):3 | ||||
| chr8:95133570-95133951 | Common:4; Rare:121 | ||||
| chr8:95269230-95269760 | Common:16; Rare:215 |