| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:146521618-146521731 | Rare:43 | ||||
| chr4:147480984-147481361 | Common:4; Rare:79 | ||||
| chr4:147617243-147617510 | Common:1; Rare:59 | ||||
| chr4:147632248-147632462 | Common:1; Rare:34 | ||||
| chr4:147683692-147683784 | Common:4; Rare:31 | ||||
| chr4:147684054-147684378 | Common:1; Rare:115 | ||||
| chr4:147731779-147732108 | Common:1; Rare:98 | ||||
| chr4:148442355-148442671 | Rare:86; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:150581734-150581962 | Rare:49 | ||||
| chr4:150582146-150582188 | Rare:8 | ||||
| chr4:151015699-151015881 | Rare:83 | ||||
| chr4:151099417-151099712 | Common:3; Rare:110 | ||||
| chr4:151226178-151226521 | Common:1; Rare:64 | ||||
| chr4:152352682-152352774 | Rare:26 | ||||
| chr4:152779729-152780190 | Common:2; Rare:118 |