| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131929078-131929271 | Common:9; Rare:55; Clinvar:1 | ||||
| chr12:132687322-132687685 | Common:4; Rare:131; Clinvar:2; Clinvar (benign):8 | ||||
| chr12:132887558-132887834 | Rare:79 | ||||
| chr13:21140390-21140666 | Rare:121 | ||||
| chr13:21176430-21176711 | Common:2; Rare:120 | ||||
| chr13:24922803-24923090 | Common:2; Rare:94; Clinvar:1 | ||||
| chr13:27251251-27251626 | Common:5; Rare:113 | ||||
| chr13:27450130-27450214 | Common:3; Rare:24 | ||||
| chr13:27450529-27450685 | Common:2; Rare:58 | ||||
| chr13:28659071-28659184 | Rare:48; Clinvar (pathogenic):1 | ||||
| chr13:30307001-30307223 | Common:4; Rare:58 | ||||
| chr13:30465824-30466117 | Common:1; Rare:91 | ||||
| chr13:30617579-30617931 | Common:1; Rare:112 | ||||
| chr13:32315426-32315552 | Rare:40; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:36297761-36297939 | Common:1; Rare:69 |