| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:8199195-8199339 | Common:1; Rare:36 | ||||
| chr4:8435983-8436155 | Common:1; Rare:32 | ||||
| chr4:8440713-8440785 | Rare:27 | ||||
| chr4:8558382-8558701 | Common:1; Rare:76 | ||||
| chr4:10116717-10117089 | Common:7; Rare:180 | ||||
| chr4:13627717-13627798 | Rare:22 | ||||
| chr4:15339830-15340007 | Rare:40 | ||||
| chr4:15427905-15428065 | Rare:21 | ||||
| chr4:15655232-15655499 | Common:2; Rare:109 | ||||
| chr4:15681554-15681869 | Common:3; Rare:110 | ||||
| chr4:17614555-17614678 | Common:2; Rare:64 | ||||
| chr4:17810687-17811043 | Common:4; Rare:111 | ||||
| chr4:18021732-18022025 | Common:2; Rare:97 | ||||
| chr4:25160388-25160611 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233843-25234074 | Rare:98 |