| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174283620-174283965 | Common:1; Rare:68 | ||||
| chr4:174522480-174522613 | Rare:42; Clinvar:2 | ||||
| chr4:177442376-177442521 | Rare:87; Clinvar:2 | ||||
| chr4:182144438-182144696 | Common:3; Rare:81 | ||||
| chr4:182917325-182917549 | Common:4; Rare:77 | ||||
| chr4:183099001-183099152 | Common:1; Rare:56 | ||||
| chr4:183504529-183504803 | Common:1; Rare:91 | ||||
| chr4:183659122-183659446 | Common:1; Rare:102 | ||||
| chr4:184474513-184474678 | Rare:37 | ||||
| chr4:184649420-184649797 | Common:4; Rare:121 | ||||
| chr4:184808336-184808669 | Rare:60 | ||||
| chr4:185396586-185396843 | Rare:83 | ||||
| chr4:185425864-185426240 | Common:3; Rare:117 | ||||
| chr4:185535453-185535632 | Common:1; Rare:59; Clinvar (benign):2 | ||||
| chr4:186191628-186191819 | Common:4; Rare:69; Clinvar:1; Clinvar (benign):4 |