| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32316319-32316436 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr13:32428104-32428514 | Rare:74 | ||||
| chr13:32538159-32538256 | Rare:23 | ||||
| chr13:32538382-32538564 | Rare:39 | ||||
| chr13:32538704-32539016 | Common:1; Rare:82 | ||||
| chr13:32539120-32539267 | Common:1; Rare:39 | ||||
| chr13:32586186-32586603 | Common:2; Rare:128 | ||||
| chr13:32586868-32587217 | Common:5; Rare:117 | ||||
| chr13:33016018-33016193 | Common:1; Rare:38 | ||||
| chr13:33285467-33285509 | Rare:12 | ||||
| chr13:33285611-33286031 | Common:2; Rare:94 | ||||
| chr13:33817966-33818270 | Common:2; Rare:135 | ||||
| chr13:36819055-36819302 | Common:1; Rare:101; Clinvar:3 | ||||
| chr13:36920111-36920170 | Rare:18; Clinvar:1 | ||||
| chr13:36920228-36920267 | Rare:16; Clinvar:1 |