| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:117085505-117085595 | Common:1; Rare:26 | ||||
| chr4:118685314-118685440 | Common:2; Rare:41 | ||||
| chr4:119212355-119212730 | Common:3; Rare:117 | ||||
| chr4:120066771-120066911 | Common:2; Rare:43 | ||||
| chr4:121801207-121801383 | Common:3; Rare:64 | ||||
| chr4:121870406-121870675 | Common:1; Rare:64; Clinvar (benign):1 | ||||
| chr4:122732432-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922897-122923145 | Common:2; Rare:74; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:124712572-124713063 | Common:1; Rare:140 | ||||
| chr4:127632767-127632985 | Common:1; Rare:54 | ||||
| chr4:127880764-127880933 | Rare:61 | ||||
| chr4:128287795-128287997 | Common:3; Rare:79 | ||||
| chr4:129093500-129093736 | Rare:72 | ||||
| chr4:133149078-133149323 | Common:2; Rare:76 | ||||
| chr4:137532380-137532704 | Common:2; Rare:54 |