| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18769828-18770097 | Common:2; Rare:59 | ||||
| chr11:19242506-19242772 | Common:1; Rare:49 | ||||
| chr11:19394544-19394688 | Rare:29 | ||||
| chr11:19432707-19432984 | Common:2; Rare:45 | ||||
| chr11:19433401-19433694 | Common:1; Rare:54 | ||||
| chr11:19442357-19442632 | Rare:48 | ||||
| chr11:19776458-19776848 | Common:6; Rare:83 | ||||
| chr11:20360822-20360944 | Common:2; Rare:16 | ||||
| chr11:22190960-22191109 | Rare:32 | ||||
| chr11:22192493-22192626 | Common:1; Rare:26 | ||||
| chr11:22624895-22625086 | Common:2; Rare:64; Clinvar:5; Clinvar (benign):4 | ||||
| chr11:22657276-22657471 | Rare:32 | ||||
| chr11:22657476-22657510 | Rare:6 | ||||
| chr11:22681332-22681524 | Common:1; Rare:31 | ||||
| chr11:22753029-22753142 | Common:1; Rare:25 |