| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47269124-47269390 | Common:1; Rare:55 | ||||
| chr11:47269550-47269830 | Common:1; Rare:98 | ||||
| chr11:47269981-47270242 | Common:2; Rare:90 | ||||
| chr11:47408511-47408670 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:47426402-47426648 | Common:1; Rare:61 | ||||
| chr11:47553020-47553335 | Common:2; Rare:114 | ||||
| chr11:47565419-47565689 | Common:3; Rare:55 | ||||
| chr11:47578940-47579106 | Rare:86; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642451-47642779 | Rare:124 | ||||
| chr11:47767067-47767642 | Common:7; Rare:195 | ||||
| chr11:47848275-47848394 | Common:1; Rare:66 | ||||
| chr11:47848540-47848662 | Common:2; Rare:25 | ||||
| chr11:57237181-57237596 | Common:5; Rare:79 | ||||
| chr11:57303651-57303755 | Common:1; Rare:21 | ||||
| chr11:57311450-57311724 | Common:1; Rare:71 |