| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124863842-124864023 | Common:1; Rare:47 | ||||
| chr12:124917630-124917812 | Rare:52 | ||||
| chr12:130839140-130839393 | Common:2; Rare:92 | ||||
| chr12:131710795-131711107 | Rare:82 | ||||
| chr12:131928993-131929280 | Common:10; Rare:86; Clinvar:1 | ||||
| chr12:132687281-132687663 | Common:3; Rare:137; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710758-132711049 | Common:3; Rare:91 | ||||
| chr12:132828827-132829166 | Common:4; Rare:117 | ||||
| chr12:132887551-132887845 | Rare:85 | ||||
| chr12:132956252-132956437 | Common:1; Rare:39 | ||||
| chr12:132986244-132986428 | Rare:39 | ||||
| chr12:133130226-133130659 | Common:7; Rare:147 | ||||
| chr13:19633427-19633751 | Common:1; Rare:121 | ||||
| chr13:19782918-19783056 | Common:1; Rare:51 | ||||
| chr13:19863538-19863866 | Common:5; Rare:121 |