| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132737257-132737342 | Common:1; Rare:20 | ||||
| chr5:132737430-132737655 | Rare:81 | ||||
| chr5:132737659-132737698 | Rare:10 | ||||
| chr5:132866560-132866978 | Common:4; Rare:132; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:132901110-132901319 | Common:1; Rare:46 | ||||
| chr5:132927565-132927802 | Common:1; Rare:37 | ||||
| chr5:132963266-132963434 | Common:1; Rare:36 | ||||
| chr5:132963466-132964058 | Common:2; Rare:174 | ||||
| chr5:133026509-133026641 | Common:1; Rare:48 | ||||
| chr5:133051862-133052380 | Common:2; Rare:162 | ||||
| chr5:133209885-133210063 | Rare:21 | ||||
| chr5:133968491-133968701 | Rare:97 | ||||
| chr5:134004627-134005045 | Common:1; Rare:129 | ||||
| chr5:134176830-134177250 | Common:4; Rare:135 | ||||
| chr5:134225518-134225593 | Common:1; Rare:26 |