| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12796468-12796712 | Common:5; Rare:63 | ||||
| chr3:13420226-13420542 | Common:1; Rare:91 | ||||
| chr3:13480040-13480318 | Common:2; Rare:64 | ||||
| chr3:14124691-14125145 | Common:4; Rare:132; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178524-14178875 | Common:2; Rare:182; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402435-14402632 | Rare:48 | ||||
| chr3:14651486-14651833 | Rare:108 | ||||
| chr3:14947209-14947563 | Common:4; Rare:156 | ||||
| chr3:14948394-14948681 | Common:2; Rare:93 | ||||
| chr3:15065184-15065364 | Common:2; Rare:73 | ||||
| chr3:15099128-15099299 | Rare:43 | ||||
| chr3:15205957-15206248 | Rare:95 | ||||
| chr3:15427471-15427741 | Common:1; Rare:92 | ||||
| chr3:15601478-15601815 | Common:4; Rare:143; Clinvar:2 | ||||
| chr3:15859777-15860230 | Common:5; Rare:134 |