| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32254580-32254612 | Rare:5 | ||||
| chr13:32315035-32315089 | Rare:11 | ||||
| chr13:32315329-32315726 | Common:2; Rare:100; Clinvar:4; Clinvar (benign):6 | ||||
| chr13:32315739-32316022 | Common:3; Rare:64; Clinvar (benign):3 | ||||
| chr13:32316315-32316392 | Rare:11; Clinvar (benign):1 | ||||
| chr13:32428107-32428402 | Rare:53 | ||||
| chr13:32538147-32538253 | Rare:26 | ||||
| chr13:32538342-32538666 | Rare:72 | ||||
| chr13:32538686-32538992 | Common:1; Rare:79 | ||||
| chr13:32539142-32539280 | Common:1; Rare:31 | ||||
| chr13:32586143-32586587 | Common:2; Rare:136 | ||||
| chr13:33285157-33285494 | Common:1; Rare:63 | ||||
| chr13:33285607-33286055 | Common:2; Rare:98 | ||||
| chr13:33817960-33818266 | Common:2; Rare:137 | ||||
| chr13:34941947-34942348 | Common:3; Rare:109 |