| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147617170-147617506 | Common:1; Rare:77 | ||||
| chr4:147684088-147684370 | Common:1; Rare:109 | ||||
| chr4:147731939-147732151 | Common:1; Rare:71 | ||||
| chr4:147732200-147732450 | Rare:89 | ||||
| chr4:148442384-148442685 | Rare:86; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:150078051-150078367 | Common:4; Rare:109 | ||||
| chr4:150078708-150078836 | Common:1; Rare:33 | ||||
| chr4:151015193-151015385 | Rare:51 | ||||
| chr4:151015681-151015885 | Rare:93 | ||||
| chr4:151016178-151016395 | Common:1; Rare:45 | ||||
| chr4:151099361-151099629 | Common:3; Rare:79 | ||||
| chr4:151324753-151325139 | Common:1; Rare:80 | ||||
| chr4:151408810-151409230 | Common:5; Rare:132 | ||||
| chr4:151760933-151761258 | Common:2; Rare:121 | ||||
| chr4:152352571-152352969 | Rare:108 |