| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:26222080-26222720 | Common:27; Rare:447 | ||||
| chr13:26253501-26254593 | Common:5; Rare:946 | ||||
| chr13:26557380-26557791 | Common:10; Rare:288 | ||||
| chr13:27171222-27172413 | Common:11; Rare:1058 | ||||
| chr13:27251203-27251692 | Common:51; Rare:883 | ||||
| chr13:27251994-27252394 | Common:3; Rare:126 | ||||
| chr13:27270401-27271352 | Common:12; Rare:657 | ||||
| chr13:27424353-27424807 | Common:25; Rare:588 | ||||
| chr13:27449419-27449819 | Common:6; Rare:97 | ||||
| chr13:27449970-27450326 | Common:21; Rare:458 | ||||
| chr13:27450310-27450840 | Common:16; Rare:605 | ||||
| chr13:27620450-27620872 | Common:10; Rare:684 | ||||
| chr13:27621209-27621609 | Common:6; Rare:165 | ||||
| chr13:27621620-27621960 | Common:27; Rare:482; Clinvar:20; Clinvar (benign):19 | ||||
| chr13:28137657-28138057 | Common:3; Rare:71 |