| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:71116197-71116229 | Rare:1 | ||||
| chr15:71116247-71116307 | Rare:8 | ||||
| chr15:71116577-71116727 | Rare:21 | ||||
| chr15:71341731-71341835 | Rare:27 | ||||
| chr15:71691521-71691816 | Common:2; Rare:47 | ||||
| chr15:72230248-72230609 | Common:3; Rare:105 | ||||
| chr15:73375997-73376187 | Rare:30 | ||||
| chr15:82372811-82372971 | Common:1; Rare:26 | ||||
| chr15:82445202-82445495 | Common:1; Rare:22 | ||||
| chr15:82750435-82750596 | Common:2; Rare:43 | ||||
| chr15:84631314-84631666 | Common:4; Rare:92 | ||||
| chr15:84827295-84827605 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:84839283-84839486 | Common:1; Rare:33 | ||||
| chr15:84840671-84841176 | Rare:133; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:85349156-85349356 | Common:3; Rare:32 |