| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150567961-150568242 | Rare:58 | ||||
| chr3:150603134-150603499 | Common:3; Rare:136 | ||||
| chr3:150703890-150704036 | Rare:51 | ||||
| chr3:150763151-150763260 | Rare:33 | ||||
| chr3:150763468-150763610 | Rare:36 | ||||
| chr3:151248912-151249311 | Rare:86 | ||||
| chr3:151384729-151385046 | Common:1; Rare:60 | ||||
| chr3:151873635-151873681 | Rare:6 | ||||
| chr3:152268439-152269212 | Common:3; Rare:260; Clinvar (benign):1 | ||||
| chr3:152269215-152269453 | Rare:72 | ||||
| chr3:152269508-152269772 | Common:2; Rare:75 | ||||
| chr3:152269898-152270042 | Common:4; Rare:39 | ||||
| chr3:152298798-152299069 | Rare:50 | ||||
| chr3:152834934-152835146 | Common:2; Rare:64 | ||||
| chr3:154121318-154121463 | Common:3; Rare:67 |