| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:31531998-31532468 | Common:5; Rare:135 | ||||
| chr5:32173814-32173969 | Rare:54 | ||||
| chr5:32174244-32174487 | Common:4; Rare:87 | ||||
| chr5:32444288-32444376 | Rare:21 | ||||
| chr5:32594884-32594907 | Rare:3 | ||||
| chr5:32710134-32710200 | Rare:8 | ||||
| chr5:32710561-32710702 | Common:1; Rare:34 | ||||
| chr5:32711012-32711536 | Common:2; Rare:98 | ||||
| chr5:32711788-32712048 | Common:1; Rare:86 | ||||
| chr5:32712059-32712142 | Rare:22 | ||||
| chr5:33440611-33441139 | Common:7; Rare:146 | ||||
| chr5:33892151-33892447 | Rare:75 | ||||
| chr5:34008018-34008219 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656159-34656521 | Common:3; Rare:89 | ||||
| chr5:34914879-34915165 | Common:1; Rare:82 |