| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:8269594-8269766 | Common:2; Rare:63 | ||||
| chr4:8440695-8440777 | Rare:32 | ||||
| chr4:10116649-10117092 | Common:8; Rare:204 | ||||
| chr4:13627670-13627839 | Common:1; Rare:51 | ||||
| chr4:15002967-15003203 | Common:2; Rare:109 | ||||
| chr4:15681466-15681879 | Common:4; Rare:143 | ||||
| chr4:17614547-17614655 | Common:2; Rare:45 | ||||
| chr4:17810702-17811012 | Common:2; Rare:95 | ||||
| chr4:24584339-24584458 | Rare:35 | ||||
| chr4:25160388-25160727 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233862-25234068 | Rare:90 | ||||
| chr4:25914051-25914296 | Common:2; Rare:103 | ||||
| chr4:26320502-26321069 | Common:1; Rare:202; Clinvar (benign):1 | ||||
| chr4:26321866-26322268 | Common:2; Rare:99 | ||||
| chr4:26857443-26857749 | Common:4; Rare:82 |