| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121696674-121696738 | Rare:13 | ||||
| chr4:121696850-121697154 | Common:5; Rare:82 | ||||
| chr4:121801263-121801411 | Common:2; Rare:49 | ||||
| chr4:122152272-122152482 | Common:2; Rare:72 | ||||
| chr4:122732417-122732824 | Common:3; Rare:128; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922933-122923145 | Common:2; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396772-123396880 | Rare:36 | ||||
| chr4:123398309-123398626 | Common:2; Rare:110 | ||||
| chr4:123399348-123399675 | Common:1; Rare:96 | ||||
| chr4:124712696-124713070 | Common:1; Rare:110 | ||||
| chr4:127880764-127880929 | Rare:61 | ||||
| chr4:128060994-128061399 | Common:1; Rare:136 | ||||
| chr4:128287779-128288016 | Common:3; Rare:93 | ||||
| chr4:128288198-128288390 | Common:5; Rare:72 | ||||
| chr4:128809517-128809829 | Common:1; Rare:98 |