| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:7067974-7068514 | Common:10; Rare:186 | ||||
| chr4:8158761-8159141 | Common:3; Rare:130 | ||||
| chr4:8199053-8199371 | Common:2; Rare:83 | ||||
| chr4:8201352-8201685 | Common:1; Rare:79 | ||||
| chr4:8228643-8228818 | Common:2; Rare:47 | ||||
| chr4:8229026-8229249 | Common:4; Rare:56 | ||||
| chr4:8428334-8428561 | Common:3; Rare:87 | ||||
| chr4:8435923-8436205 | Common:1; Rare:50 | ||||
| chr4:8440258-8440283 | Common:1; Rare:4 | ||||
| chr4:8440637-8440841 | Rare:77 | ||||
| chr4:10018949-10019137 | Common:1; Rare:75; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:10019139-10019200 | Rare:9 | ||||
| chr4:10019254-10019360 | Common:1; Rare:25 | ||||
| chr4:10115905-10116136 | Common:4; Rare:83 | ||||
| chr4:10116691-10117117 | Common:11; Rare:209 |