| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68271393-68271793 | Common:1; Rare:122 | ||||
| chr11:68271850-68272330 | Common:6; Rare:421 | ||||
| chr11:68312180-68312760 | Common:3; Rare:328; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:68313163-68313681 | Common:2; Rare:111 | ||||
| chr11:68459988-68460337 | Common:5; Rare:222 | ||||
| chr11:68460461-68460865 | Common:9; Rare:337 | ||||
| chr11:68461275-68461625 | Common:4; Rare:101 | ||||
| chr11:68684437-68684588 | Common:1; Rare:45 | ||||
| chr11:68751348-68751702 | Common:3; Rare:195 | ||||
| chr11:68818151-68818651 | Common:6; Rare:146 | ||||
| chr11:68839208-68839582 | Common:5; Rare:206 | ||||
| chr11:68841686-68842251 | Common:5; Rare:274; Clinvar (benign):8 | ||||
| chr11:68843803-68844240 | Common:5; Rare:196 | ||||
| chr11:68903730-68903990 | Common:14; Rare:297; Clinvar:8; Clinvar (benign):20 | ||||
| chr11:69048701-69049040 | Common:12; Rare:225 |