| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:149987831-149987838 | Rare:2 | ||||
| chr4:149988013-149988341 | Common:4; Rare:68 | ||||
| chr4:150039859-150040070 | Rare:40 | ||||
| chr4:150217421-150217470 | Common:1; Rare:4 | ||||
| chr4:150224912-150225148 | Common:1; Rare:29 | ||||
| chr4:150316389-150316580 | Rare:29 | ||||
| chr4:150356319-150356350 | Rare:4 | ||||
| chr4:150385668-150385814 | Common:1; Rare:22 | ||||
| chr4:150546430-150546590 | Common:2; Rare:24 | ||||
| chr4:150594137-150594292 | Rare:21 | ||||
| chr4:150594502-150594525 | Rare:3 | ||||
| chr4:150598633-150598718 | Rare:16 | ||||
| chr4:150598961-150599210 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:151014383-151014688 | Rare:90; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:151106206-151106501 | Rare:63 |