| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139198284-139198527 | Rare:82; Clinvar (benign):1 | ||||
| chr5:139273950-139274153 | Rare:93 | ||||
| chr5:139293918-139294018 | Rare:28 | ||||
| chr5:139341796-139341985 | Common:1; Rare:53 | ||||
| chr5:139395056-139395216 | Rare:40 | ||||
| chr5:139403986-139404185 | Rare:68 | ||||
| chr5:139439452-139439597 | Common:1; Rare:40 | ||||
| chr5:139561100-139561576 | Common:1; Rare:197 | ||||
| chr5:139561727-139561800 | Rare:31 | ||||
| chr5:140107608-140107815 | Rare:69 | ||||
| chr5:140303059-140303153 | Common:1; Rare:34 | ||||
| chr5:140346600-140346736 | Common:1; Rare:41 | ||||
| chr5:140547510-140547719 | Common:1; Rare:47 | ||||
| chr5:140557417-140557536 | Common:1; Rare:76 | ||||
| chr5:140564296-140564470 | Common:1; Rare:49 |