| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115841472-115842105 | Common:8; Rare:275 | ||||
| chr5:116084965-116085058 | Common:2; Rare:46 | ||||
| chr5:116574810-116574829 | Rare:7 | ||||
| chr5:119070872-119071207 | Common:3; Rare:106 | ||||
| chr5:119071337-119071477 | Rare:63 | ||||
| chr5:119268596-119268902 | Common:1; Rare:89 | ||||
| chr5:119355829-119356021 | Common:2; Rare:49 | ||||
| chr5:122845309-122845621 | Common:3; Rare:106 | ||||
| chr5:123036648-123036902 | Common:2; Rare:62 | ||||
| chr5:126423343-126423618 | Rare:79 | ||||
| chr5:126595142-126595327 | Common:3; Rare:88; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr5:126776907-126777184 | Common:1; Rare:108; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:127030476-127030793 | Common:3; Rare:81 | ||||
| chr5:127073471-127073523 | Common:1; Rare:11 | ||||
| chr5:128083619-128083766 | Common:2; Rare:61 |