| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27450503-27450643 | Common:2; Rare:59 | ||||
| chr13:27620469-27620829 | Common:2; Rare:120 | ||||
| chr13:28138139-28138234 | Common:1; Rare:28 | ||||
| chr13:28658937-28659001 | Rare:15 | ||||
| chr13:28659042-28659068 | Rare:14 | ||||
| chr13:28659076-28659194 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr13:28718814-28719123 | Common:1; Rare:78 | ||||
| chr13:29595675-29595897 | Common:2; Rare:85 | ||||
| chr13:30307001-30307197 | Common:4; Rare:46 | ||||
| chr13:30307390-30307597 | Common:2; Rare:71 | ||||
| chr13:30464195-30464386 | Common:1; Rare:53 | ||||
| chr13:30464868-30464984 | Common:1; Rare:36 | ||||
| chr13:30616972-30617162 | Rare:33 | ||||
| chr13:30617233-30618046 | Common:1; Rare:246 | ||||
| chr13:30735395-30735663 | Common:2; Rare:64 |