| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138610477-138610877 | Common:5; Rare:98 | ||||
| chr5:138611338-138611454 | Common:3; Rare:28 | ||||
| chr5:138753251-138753483 | Common:2; Rare:82 | ||||
| chr5:138753570-138754365 | Common:7; Rare:302; Clinvar (benign):4 | ||||
| chr5:138827410-138827810 | Rare:135; Clinvar (benign):2 | ||||
| chr5:139198240-139198590 | Common:1; Rare:109; Clinvar (benign):1 | ||||
| chr5:139273930-139274150 | Rare:101 | ||||
| chr5:139293516-139293754 | Rare:79 | ||||
| chr5:139294369-139294576 | Rare:78 | ||||
| chr5:139294659-139294795 | Rare:28 | ||||
| chr5:139341681-139341887 | Common:1; Rare:46 | ||||
| chr5:139342169-139342516 | Common:3; Rare:121 | ||||
| chr5:139403973-139404226 | Rare:88 | ||||
| chr5:139439415-139439648 | Common:2; Rare:62 | ||||
| chr5:139561435-139561559 | Rare:54 |