| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99087949-99088171 | Common:2; Rare:49 | ||||
| chr13:102394467-102394660 | Common:1; Rare:76 | ||||
| chr13:109229703-109229999 | Common:2; Rare:49 | ||||
| chr13:109265124-109265419 | Common:4; Rare:68 | ||||
| chr13:109265896-109266006 | Common:1; Rare:25 | ||||
| chr13:109267053-109267115 | Common:1; Rare:17 | ||||
| chr13:109267327-109267645 | Common:5; Rare:55 | ||||
| chr13:109267763-109267795 | Rare:7 | ||||
| chr13:109268695-109269164 | Common:9; Rare:85 | ||||
| chr13:109269227-109269574 | Common:3; Rare:65 | ||||
| chr13:109269576-109269709 | Common:2; Rare:31 | ||||
| chr13:109782278-109782340 | Rare:31 | ||||
| chr13:109782728-109782998 | Common:7; Rare:118; Clinvar:1 | ||||
| chr13:109785227-109785586 | Common:2; Rare:114 | ||||
| chr13:110205351-110205531 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |