| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129448320-129448348 | Rare:4 | ||||
| chr3:129469176-129469369 | Common:2; Rare:51 | ||||
| chr3:130111429-130111761 | Common:3; Rare:85 | ||||
| chr3:130112407-130112568 | Common:3; Rare:46 | ||||
| chr3:131361579-131361946 | Common:3; Rare:113 | ||||
| chr3:131363292-131363649 | Common:5; Rare:52 | ||||
| chr3:132492216-132492521 | Common:2; Rare:71 | ||||
| chr3:132686290-132686491 | Rare:48; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:132689171-132689481 | Rare:72; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr3:133491075-133491322 | Rare:53 | ||||
| chr3:134201412-134201707 | Rare:58 | ||||
| chr3:134361682-134362027 | Common:1; Rare:97 | ||||
| chr3:136049129-136049359 | Rare:53 | ||||
| chr3:136484297-136484390 | Common:1; Rare:38 | ||||
| chr3:137999436-137999791 | Common:2; Rare:73 |