| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:13514606-13514780 | Common:2; Rare:44 | ||||
| chr8:13514788-13514962 | Rare:37 | ||||
| chr8:15540143-15540469 | Common:5; Rare:127; Clinvar:12; Clinvar (benign):1 | ||||
| chr8:17246583-17247048 | Common:5; Rare:196 | ||||
| chr8:17676325-17676537 | Common:3; Rare:64 | ||||
| chr8:17801080-17801344 | Common:7; Rare:99 | ||||
| chr8:17922616-17922929 | Common:4; Rare:116 | ||||
| chr8:18084771-18084880 | Common:1; Rare:52; Clinvar (benign):1 | ||||
| chr8:18084921-18085038 | Rare:27 | ||||
| chr8:19817114-19817416 | Common:5; Rare:92 | ||||
| chr8:20197202-20197440 | Common:1; Rare:115 | ||||
| chr8:21913682-21913854 | Rare:49 | ||||
| chr8:22102635-22102891 | Rare:76 | ||||
| chr8:22245024-22245150 | Rare:66 | ||||
| chr8:22367135-22367324 | Common:5; Rare:75 |