| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57998928-57999100 | Rare:22 | ||||
| chr3:58009166-58009303 | Common:1; Rare:29 | ||||
| chr3:58073964-58074144 | Common:1; Rare:34 | ||||
| chr3:58111740-58111874 | Common:1; Rare:27; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:58116154-58116505 | Common:3; Rare:76 | ||||
| chr3:58203003-58203172 | Common:3; Rare:32 | ||||
| chr3:58349869-58350045 | Common:1; Rare:35 | ||||
| chr3:58355301-58355402 | Rare:23 | ||||
| chr3:58868193-58868309 | Rare:18 | ||||
| chr3:59451399-59451731 | Common:4; Rare:56 | ||||
| chr3:61236639-61236873 | Common:2; Rare:36 | ||||
| chr3:61250046-61250348 | Rare:84 | ||||
| chr3:61560701-61560817 | Common:1; Rare:37 | ||||
| chr3:61637505-61637681 | Rare:50 | ||||
| chr3:62723548-62723805 | Common:3; Rare:51 |