| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:130850996-130851065 | Rare:13 | ||||
| chr3:130893463-130893514 | Common:1; Rare:6 | ||||
| chr3:130893843-130894275 | Common:3; Rare:128 | ||||
| chr3:131026553-131026910 | Common:2; Rare:79 | ||||
| chr3:131381383-131381904 | Common:4; Rare:153 | ||||
| chr3:131502782-131503104 | Common:1; Rare:118 | ||||
| chr3:132417120-132417676 | Common:6; Rare:191 | ||||
| chr3:132417844-132418112 | Common:2; Rare:90 | ||||
| chr3:132659453-132659496 | Rare:5 | ||||
| chr3:132659785-132659999 | Common:3; Rare:48 | ||||
| chr3:132660057-132660463 | Common:2; Rare:85 | ||||
| chr3:132660703-132660794 | Common:1; Rare:29 | ||||
| chr3:132660931-132660975 | Rare:6 | ||||
| chr3:133448532-133448878 | Rare:84; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:133573093-133573320 | Common:2; Rare:63 |