| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75673076-75673222 | Rare:35 | ||||
| chr4:75673282-75673692 | Common:1; Rare:158 | ||||
| chr4:75724375-75724719 | Common:1; Rare:95 | ||||
| chr4:75724731-75724856 | Common:1; Rare:51 | ||||
| chr4:76148377-76148556 | Common:3; Rare:57 | ||||
| chr4:76213676-76213988 | Common:2; Rare:101 | ||||
| chr4:76949599-76949895 | Common:1; Rare:91 | ||||
| chr4:77075934-77076056 | Rare:73 | ||||
| chr4:77862659-77862872 | Common:3; Rare:79 | ||||
| chr4:78057459-78057605 | Common:2; Rare:32 | ||||
| chr4:78939245-78939515 | Common:2; Rare:113 | ||||
| chr4:82373936-82374188 | Common:2; Rare:76 | ||||
| chr4:82429377-82429572 | Rare:121; Clinvar:5; Clinvar (benign):3 | ||||
| chr4:82430463-82430634 | Rare:60 | ||||
| chr4:82900477-82900732 | Rare:73 |