| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33114414-33114556 | Common:1; Rare:58; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:33277295-33277509 | Common:3; Rare:63 | ||||
| chr3:33440348-33440524 | Common:1; Rare:50 | ||||
| chr3:33718153-33718329 | Rare:84 | ||||
| chr3:33798514-33798936 | Common:3; Rare:151 | ||||
| chr3:33798991-33799096 | Rare:37 | ||||
| chr3:33828786-33829090 | Rare:64 | ||||
| chr3:36993035-36993658 | Common:2; Rare:220; Clinvar:47; Clinvar (benign):21; Clinvar (pathogenic):4 | ||||
| chr3:37176055-37176393 | Common:1; Rare:94 | ||||
| chr3:37243036-37243433 | Common:5; Rare:101 | ||||
| chr3:37861710-37861803 | Rare:27 | ||||
| chr3:38024510-38024648 | Common:1; Rare:52 | ||||
| chr3:38137043-38137447 | Common:1; Rare:99 | ||||
| chr3:38164949-38165272 | Common:1; Rare:79 | ||||
| chr3:38165462-38165865 | Common:1; Rare:140 |