| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66480620-66480787 | Common:1; Rare:40 | ||||
| chr11:66510547-66510741 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr11:66545951-66546406 | Common:5; Rare:123 | ||||
| chr11:66592998-66593278 | Common:1; Rare:99 | ||||
| chr11:66616136-66616236 | Rare:21 | ||||
| chr11:66616329-66616684 | Common:2; Rare:112 | ||||
| chr11:66616950-66617189 | Common:1; Rare:81 | ||||
| chr11:66618766-66618895 | Rare:29 | ||||
| chr11:66638356-66638772 | Common:4; Rare:183 | ||||
| chr11:66677579-66677704 | Rare:32 | ||||
| chr11:66677781-66678265 | Common:1; Rare:154 | ||||
| chr11:66744445-66744998 | Common:5; Rare:163 | ||||
| chr11:66842880-66843011 | Common:1; Rare:58 | ||||
| chr11:66843201-66843530 | Common:6; Rare:172 | ||||
| chr11:66843612-66843766 | Common:1; Rare:68 |