| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126355526-126355742 | Common:2; Rare:56 | ||||
| chr11:128522263-128522596 | Common:3; Rare:105 | ||||
| chr11:128692805-128692978 | Rare:44 | ||||
| chr11:128692983-128693017 | Common:1; Rare:4 | ||||
| chr11:128693462-128693789 | Common:5; Rare:85 | ||||
| chr11:128693797-128694232 | Common:2; Rare:81 | ||||
| chr11:130002790-130002973 | Common:3; Rare:33 | ||||
| chr11:130069624-130070079 | Common:2; Rare:161 | ||||
| chr11:130314417-130314509 | Common:1; Rare:29 | ||||
| chr11:134253298-134253592 | Common:2; Rare:97; Clinvar (benign):1 | ||||
| chr12:389249-389368 | Rare:44 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:991119-991318 | Common:3; Rare:93 | ||||
| chr12:2004408-2004669 | Common:2; Rare:89 | ||||
| chr12:2876925-2877278 | Common:1; Rare:113 |