| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65873541-65873830 | Common:3; Rare:92 | ||||
| chr11:65888073-65888107 | Rare:17 | ||||
| chr11:65888392-65888725 | Common:1; Rare:112 | ||||
| chr11:65890431-65890719 | Common:5; Rare:90 | ||||
| chr11:65900337-65900821 | Common:5; Rare:100 | ||||
| chr11:65918481-65918638 | Common:3; Rare:36 | ||||
| chr11:65918768-65918805 | Common:1; Rare:15 | ||||
| chr11:65918830-65918852 | Rare:3 | ||||
| chr11:65918934-65919557 | Common:2; Rare:236 | ||||
| chr11:65919851-65919897 | Rare:21 | ||||
| chr11:65961377-65961820 | Common:1; Rare:140 | ||||
| chr11:65962018-65962250 | Common:5; Rare:81 | ||||
| chr11:66002065-66002818 | Common:4; Rare:210; Clinvar:8; Clinvar (benign):3 | ||||
| chr11:66002893-66003188 | Common:4; Rare:73 | ||||
| chr11:66011361-66011504 | Common:1; Rare:17 |