| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:18084921-18084997 | Rare:21 | ||||
| chr8:19013629-19013961 | Common:5; Rare:98 | ||||
| chr8:19313568-19313708 | Common:1; Rare:42 | ||||
| chr8:19757881-19758183 | Common:1; Rare:51 | ||||
| chr8:19817074-19817533 | Common:8; Rare:161 | ||||
| chr8:20197202-20197427 | Common:1; Rare:107 | ||||
| chr8:21912458-21912617 | Common:2; Rare:58 | ||||
| chr8:21919423-21919773 | Common:2; Rare:132 | ||||
| chr8:22089079-22089226 | Rare:55 | ||||
| chr8:22165380-22165417 | Common:1; Rare:11; Clinvar (benign):1 | ||||
| chr8:22231971-22231988 | |||||
| chr8:22232003-22232111 | Rare:32 | ||||
| chr8:22245022-22245192 | Common:1; Rare:83 | ||||
| chr8:22367161-22367331 | Common:5; Rare:71 | ||||
| chr8:22412200-22412398 | Rare:41 |