| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:12436347-12436520 | Common:4; Rare:34 | ||||
| chr8:12754039-12754202 | Common:1; Rare:63 | ||||
| chr8:13133237-13133556 | Common:11; Rare:86 | ||||
| chr8:17246589-17247032 | Common:5; Rare:191 | ||||
| chr8:17413305-17413511 | Common:3; Rare:108 | ||||
| chr8:17496874-17497178 | Common:5; Rare:124 | ||||
| chr8:17697479-17697716 | Common:1; Rare:49 | ||||
| chr8:17801075-17801344 | Common:7; Rare:101 | ||||
| chr8:17922606-17922929 | Common:4; Rare:120 | ||||
| chr8:18084820-18084864 | Common:1; Rare:16; Clinvar (benign):1 | ||||
| chr8:18084921-18085046 | Rare:28 | ||||
| chr8:19013629-19013983 | Common:5; Rare:107 | ||||
| chr8:19313563-19313772 | Common:3; Rare:62 | ||||
| chr8:19817049-19817406 | Common:5; Rare:111 | ||||
| chr8:20197209-20197410 | Common:1; Rare:92 |