| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:129279490-129279765 | Common:4; Rare:119 | ||||
| chr11:129895535-129895687 | Common:2; Rare:57 | ||||
| chr11:130002741-130002949 | Common:2; Rare:42 | ||||
| chr11:130069607-130070079 | Common:2; Rare:171 | ||||
| chr11:130314395-130314520 | Common:1; Rare:42 | ||||
| chr11:130916411-130916658 | Common:6; Rare:74 | ||||
| chr11:131911184-131911209 | Rare:12 | ||||
| chr11:131911294-131911644 | Common:2; Rare:120 | ||||
| chr11:132943097-132943197 | Rare:40 | ||||
| chr11:133532308-133532543 | Common:2; Rare:53 | ||||
| chr11:134068984-134069086 | Rare:60; Clinvar (pathogenic):1 | ||||
| chr11:134253098-134253592 | Common:2; Rare:148; Clinvar (benign):1 | ||||
| chr11:134276191-134276376 | Common:3; Rare:39 | ||||
| chr12:389071-389377 | Common:5; Rare:158 | ||||
| chr12:389483-389640 | Common:5; Rare:67 |