| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126355532-126355790 | Common:1; Rare:72 | ||||
| chr11:128522388-128522602 | Common:3; Rare:74 | ||||
| chr11:129895535-129895682 | Common:2; Rare:56 | ||||
| chr11:129947555-129947760 | Rare:33 | ||||
| chr11:130003229-130003367 | Rare:62 | ||||
| chr11:130314417-130314495 | Common:1; Rare:22 | ||||
| chr11:130916438-130916642 | Common:5; Rare:60 | ||||
| chr11:134223922-134224233 | Common:2; Rare:110 | ||||
| chr11:134253290-134253586 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr12:389249-389364 | Rare:40 | ||||
| chr12:389533-389667 | Common:5; Rare:58 | ||||
| chr12:401446-401669 | Rare:60 | ||||
| chr12:752306-752587 | Common:1; Rare:85 | ||||
| chr12:991128-991318 | Common:2; Rare:89 | ||||
| chr12:2812507-2812713 | Common:1; Rare:49 |