| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:30626568-30626781 | Common:1; Rare:35 | ||||
| chr15:30903601-30903999 | Common:3; Rare:187 | ||||
| chr15:30990899-30991358 | Common:6; Rare:195 | ||||
| chr15:30991464-30991920 | Common:13; Rare:379 | ||||
| chr15:30991860-30992100 | Common:3; Rare:125 | ||||
| chr15:31326310-31326895 | Common:11; Rare:538 | ||||
| chr15:31327933-31328177 | Common:1; Rare:147 | ||||
| chr15:31870608-31871100 | Common:1; Rare:357 | ||||
| chr15:32615070-32615536 | Common:16; Rare:334 | ||||
| chr15:32677281-32677540 | Rare:43 | ||||
| chr15:32677475-32677580 | Rare:24 | ||||
| chr15:33067518-33068371 | Common:10; Rare:629; Clinvar:4; Clinvar (benign):2 | ||||
| chr15:33068657-33069036 | Common:2; Rare:93 | ||||
| chr15:33194633-33195033 | Common:6; Rare:351 | ||||
| chr15:34038400-34039258 | Common:21; Rare:500 |