| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153466221-153466391 | Common:3; Rare:72 | ||||
| chr4:154550304-154550530 | Common:2; Rare:75 | ||||
| chr4:158671874-158672139 | Common:3; Rare:63 | ||||
| chr4:158672205-158672358 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:158723355-158723446 | Rare:42 | ||||
| chr4:163166860-163167007 | Common:2; Rare:55 | ||||
| chr4:163613465-163613644 | Common:1; Rare:42 | ||||
| chr4:168318747-168318885 | Rare:27 | ||||
| chr4:168480484-168480639 | Rare:20 | ||||
| chr4:169010237-169010485 | Common:1; Rare:74 | ||||
| chr4:169612554-169612797 | Common:4; Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169619909-169620206 | Common:2; Rare:62 | ||||
| chr4:169620391-169620598 | Common:2; Rare:79 | ||||
| chr4:169660032-169660261 | Common:1; Rare:44 | ||||
| chr4:173168527-173168811 | Common:2; Rare:78 |