| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132956252-132956437 | Common:1; Rare:39 | ||||
| chr12:132986238-132986428 | Rare:40 | ||||
| chr12:133037220-133037554 | Common:4; Rare:72 | ||||
| chr12:133080253-133080454 | Common:5; Rare:62 | ||||
| chr12:133080728-133080950 | Rare:70 | ||||
| chr12:133130226-133130662 | Common:7; Rare:147 | ||||
| chr13:19633527-19633751 | Common:1; Rare:87 | ||||
| chr13:19782918-19783088 | Common:2; Rare:62 | ||||
| chr13:20525784-20525969 | Common:1; Rare:71 | ||||
| chr13:21140377-21140636 | Rare:115 | ||||
| chr13:21176468-21176708 | Common:2; Rare:105 | ||||
| chr13:21459187-21459507 | Common:1; Rare:113 | ||||
| chr13:21670971-21671162 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:23579247-23579461 | Common:3; Rare:68 | ||||
| chr13:23889256-23889460 | Rare:68 |