| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143817700-143817904 | Rare:49 | ||||
| chr8:143935096-143935270 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):5 | ||||
| chr8:145002825-145003038 | Common:2; Rare:76 | ||||
| chr9:693607-693714 | Rare:34 | ||||
| chr9:4293785-4293880 | Rare:24 | ||||
| chr9:5509592-5509949 | Common:4; Rare:64 | ||||
| chr9:7799465-7799500 | Rare:21 | ||||
| chr9:12814319-12814702 | Common:6; Rare:85 | ||||
| chr9:12815980-12816305 | Common:6; Rare:63 | ||||
| chr9:12817707-12817878 | Common:1; Rare:30 | ||||
| chr9:15469269-15469579 | Common:2; Rare:79 | ||||
| chr9:15469938-15470113 | Rare:57 | ||||
| chr9:16726781-16726944 | Common:1; Rare:40 | ||||
| chr9:16986017-16986031 | Rare:1 | ||||
| chr9:17003726-17004083 | Common:2; Rare:81 |