| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126303869-126304081 | Rare:90 | ||||
| chr11:128522262-128522540 | Common:1; Rare:84 | ||||
| chr11:128891136-128891308 | Common:1; Rare:54 | ||||
| chr11:129279490-129279741 | Common:3; Rare:108 | ||||
| chr11:129895535-129895663 | Common:2; Rare:47 | ||||
| chr11:130069624-130070037 | Common:2; Rare:146 | ||||
| chr11:130314417-130314520 | Common:1; Rare:34 | ||||
| chr11:130448491-130448647 | Rare:42 | ||||
| chr11:134253325-134253594 | Common:2; Rare:85; Clinvar (benign):1 | ||||
| chr12:389242-389398 | Common:1; Rare:59 | ||||
| chr12:401446-401645 | Rare:53 | ||||
| chr12:643624-643867 | Common:2; Rare:47 | ||||
| chr12:991101-991318 | Common:3; Rare:99 | ||||
| chr12:2004418-2004669 | Common:2; Rare:82 | ||||
| chr12:2812580-2812713 | Common:1; Rare:41 |