| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124623109-124623348 | Common:1; Rare:71 | ||||
| chr11:124673327-124673497 | Common:1; Rare:42 | ||||
| chr11:124673624-124674251 | Common:5; Rare:159 | ||||
| chr11:124739829-124739960 | Rare:35 | ||||
| chr11:124799767-124799935 | Rare:57 | ||||
| chr11:124799992-124800070 | Rare:16 | ||||
| chr11:124800330-124800538 | Common:1; Rare:81 | ||||
| chr11:124800601-124800739 | Common:1; Rare:27 | ||||
| chr11:124800828-124800908 | Common:1; Rare:13 | ||||
| chr11:124876318-124876569 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:124876583-124876759 | Common:1; Rare:25 | ||||
| chr11:124876763-124876932 | Common:2; Rare:39 | ||||
| chr11:124877417-124877646 | Common:2; Rare:80; Clinvar:2 | ||||
| chr11:124896795-124897023 | Rare:66 | ||||
| chr11:124897186-124897255 | Common:2; Rare:18 |