| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:135399084-135399337 | Rare:65 | ||||
| chr5:136132692-136132972 | Common:1; Rare:93 | ||||
| chr5:137735822-137736140 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:137754329-137754519 | Rare:62 | ||||
| chr5:137889320-137889408 | Common:1; Rare:31 | ||||
| chr5:138032706-138032780 | Common:1; Rare:16 | ||||
| chr5:138032995-138033180 | Common:1; Rare:63 | ||||
| chr5:138178604-138178756 | Rare:35 | ||||
| chr5:138178927-138179195 | Common:3; Rare:55 | ||||
| chr5:138213292-138213350 | Rare:19 | ||||
| chr5:138331765-138332151 | Common:2; Rare:93 | ||||
| chr5:138337975-138338297 | Common:2; Rare:125 | ||||
| chr5:138542914-138543585 | Common:3; Rare:209 | ||||
| chr5:138543714-138543746 | Rare:4 | ||||
| chr5:138575673-138575951 | Rare:78 |