| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:26609501-26609719 | Rare:47 | ||||
| chr8:26609904-26610026 | Rare:21 | ||||
| chr8:26611676-26611802 | Common:2; Rare:19 | ||||
| chr8:27309464-27309701 | Rare:37 | ||||
| chr8:27598212-27598417 | Rare:54 | ||||
| chr8:29060777-29061031 | Common:1; Rare:56 | ||||
| chr8:30305688-30305865 | Rare:35 | ||||
| chr8:30502936-30503207 | Common:4; Rare:41 | ||||
| chr8:30560084-30560258 | Common:1; Rare:38 | ||||
| chr8:30563380-30563443 | Rare:25 | ||||
| chr8:37748002-37748068 | Rare:28 | ||||
| chr8:38382959-38383057 | Common:1; Rare:23 | ||||
| chr8:38405419-38405451 | Rare:4 | ||||
| chr8:38408178-38408237 | Rare:23 | ||||
| chr8:38414558-38414799 | Rare:63; Clinvar:2; Clinvar (pathogenic):1 |