| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65893146-65893433 | Common:2; Rare:74 | ||||
| chr11:95150980-95151200 | Common:1; Rare:55 | ||||
| chr11:102796645-102797158 | Common:1; Rare:157 | ||||
| chr11:109946379-109946573 | Common:1; Rare:48 | ||||
| chr11:118241110-118241354 | Rare:45 | ||||
| chr11:118791680-118791810 | Common:1; Rare:39 | ||||
| chr11:119314487-119314750 | Common:1; Rare:85 | ||||
| chr11:121236519-121236809 | Common:4; Rare:59 | ||||
| chr11:124895471-124895837 | Common:4; Rare:131; Clinvar (pathogenic):1 | ||||
| chr12:3300147-3300331 | Common:2; Rare:56 | ||||
| chr12:6121277-6121515 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:6123446-6123543 | Rare:22 | ||||
| chr12:6172243-6172372 | Common:1; Rare:22 | ||||
| chr12:6182251-6182585 | Common:4; Rare:65 | ||||
| chr12:6770189-6770523 | Rare:94 |