| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70203101-70203343 | Common:4; Rare:94 | ||||
| chr11:70398331-70398596 | Common:2; Rare:89 | ||||
| chr11:71448338-71448697 | Common:4; Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787350-71787546 | Common:12; Rare:82 | ||||
| chr11:71928893-71929058 | Common:1; Rare:55 | ||||
| chr11:72041094-72041236 | Common:1; Rare:22 | ||||
| chr11:72080471-72080812 | Common:1; Rare:75; Clinvar:5 | ||||
| chr11:72112223-72112520 | Rare:76 | ||||
| chr11:72112655-72112823 | Common:1; Rare:74 | ||||
| chr11:72223774-72223927 | Rare:45 | ||||
| chr11:72434467-72434727 | Common:4; Rare:72; Clinvar (benign):1 | ||||
| chr11:72722306-72722648 | Rare:73 | ||||
| chr11:72814318-72814432 | Rare:37 | ||||
| chr11:73598035-73598287 | Common:3; Rare:64 | ||||
| chr11:73787796-73787953 | Common:1; Rare:39 |