| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33258039-33258364 | Common:2; Rare:109 | ||||
| chr11:33736349-33736605 | Common:3; Rare:75 | ||||
| chr11:34052156-34052510 | Common:4; Rare:162 | ||||
| chr11:34438784-34439023 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr11:34620933-34621122 | Common:2; Rare:34 | ||||
| chr11:34624158-34624290 | Common:1; Rare:27 | ||||
| chr11:34916311-34916650 | Common:9; Rare:139; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr11:35139013-35139354 | Common:1; Rare:94 | ||||
| chr11:35200854-35201105 | Rare:51 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358802-43358983 | Rare:86 | ||||
| chr11:44565273-44565720 | Common:3; Rare:114 | ||||
| chr11:45847215-45847487 | Common:2; Rare:109 | ||||
| chr11:45917827-45918190 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46617183-46617585 | Common:5; Rare:113 |