| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:24512145-24512389 | Common:2; Rare:46 | ||||
| chr13:24512391-24512929 | Common:5; Rare:140 | ||||
| chr13:24680296-24680567 | Common:2; Rare:70 | ||||
| chr13:24922446-24922583 | Common:1; Rare:35 | ||||
| chr13:24922640-24923347 | Common:7; Rare:199; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:25287218-25287641 | Common:3; Rare:136 | ||||
| chr13:25301440-25301870 | Common:4; Rare:166 | ||||
| chr13:26221707-26222075 | Common:2; Rare:110 | ||||
| chr13:26222129-26222605 | Common:7; Rare:124 | ||||
| chr13:26253722-26253994 | Rare:65 | ||||
| chr13:26254056-26254657 | Common:4; Rare:155 | ||||
| chr13:27171002-27171286 | Common:3; Rare:71 | ||||
| chr13:27171330-27171527 | Common:1; Rare:42 | ||||
| chr13:27171734-27172123 | Common:1; Rare:144 | ||||
| chr13:27251096-27251751 | Common:9; Rare:202 |