| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124762282-124762447 | Rare:42 | ||||
| chr11:124800406-124800460 | Rare:17 | ||||
| chr11:124953989-124954144 | Common:3; Rare:44 | ||||
| chr11:125063123-125063305 | Common:2; Rare:49 | ||||
| chr11:125592510-125592930 | Common:6; Rare:137 | ||||
| chr11:125625864-125626003 | Rare:45 | ||||
| chr11:125887495-125887727 | Common:2; Rare:72 | ||||
| chr11:126211623-126211819 | Rare:90 | ||||
| chr11:126268746-126269209 | Common:2; Rare:177; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126304016-126304083 | Rare:37 | ||||
| chr11:126405400-126405664 | Common:2; Rare:47 | ||||
| chr11:126405907-126406130 | Common:3; Rare:55 | ||||
| chr11:128522222-128522597 | Common:3; Rare:114 | ||||
| chr11:128694005-128694142 | Rare:26 | ||||
| chr11:129279476-129279738 | Common:3; Rare:109 |