| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:77027137-77027280 | Common:5; Rare:46 | ||||
| chr13:77327060-77327166 | Rare:47 | ||||
| chr13:77918537-77918953 | Common:2; Rare:96; Clinvar (benign):2 | ||||
| chr13:77919131-77919599 | Common:1; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:77919674-77919727 | Rare:14 | ||||
| chr13:79405720-79405932 | Common:1; Rare:68 | ||||
| chr13:79406190-79406339 | Common:4; Rare:48 | ||||
| chr13:79481019-79481474 | Common:2; Rare:179 | ||||
| chr13:94596139-94596335 | Common:2; Rare:63 | ||||
| chr13:94601592-94601930 | Common:3; Rare:100 | ||||
| chr13:95676887-95677268 | Common:4; Rare:145 | ||||
| chr13:96053331-96053608 | Common:3; Rare:119 | ||||
| chr13:97222095-97222497 | Rare:76 | ||||
| chr13:98576172-98576321 | Common:1; Rare:51 | ||||
| chr13:99200663-99200921 | Common:6; Rare:120 |