| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32174236-32174401 | Common:1; Rare:62 | ||||
| chr5:32531658-32531865 | Common:1; Rare:40 | ||||
| chr5:32710330-32710688 | Common:3; Rare:73 | ||||
| chr5:33440632-33441104 | Common:7; Rare:136 | ||||
| chr5:34656162-34656488 | Common:3; Rare:82 | ||||
| chr5:34915454-34915775 | Common:1; Rare:93 | ||||
| chr5:36151885-36152196 | Rare:100 | ||||
| chr5:36876650-36876844 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr5:37371018-37371383 | Common:2; Rare:96 | ||||
| chr5:38845716-38846094 | Common:2; Rare:99 | ||||
| chr5:40835178-40835371 | Common:2; Rare:79 | ||||
| chr5:43483837-43483916 | Common:1; Rare:31 | ||||
| chr5:43603096-43603219 | Rare:28 | ||||
| chr5:44808743-44808965 | Common:2; Rare:71 | ||||
| chr5:50667751-50668120 | Common:1; Rare:111 |