| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34839265-34839404 | Common:2; Rare:41 | ||||
| chr5:34915450-34915761 | Common:1; Rare:84 | ||||
| chr5:35617841-35617928 | Rare:20 | ||||
| chr5:36151838-36152140 | Rare:79 | ||||
| chr5:36876655-36876900 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371046-37371207 | Rare:57 | ||||
| chr5:37379179-37379364 | Rare:47 | ||||
| chr5:38445256-38445570 | Common:1; Rare:55 | ||||
| chr5:38557225-38557375 | Rare:40 | ||||
| chr5:38557436-38557710 | Common:2; Rare:50 | ||||
| chr5:38845739-38846053 | Common:2; Rare:83 | ||||
| chr5:39074276-39074495 | Common:1; Rare:102 | ||||
| chr5:40679711-40679938 | Common:1; Rare:50 | ||||
| chr5:40755901-40756111 | Rare:59 | ||||
| chr5:40798141-40798407 | Common:1; Rare:103 |