| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:39161818-39161908 | Common:2; Rare:32 | ||||
| chr11:43458338-43458363 | Rare:4 | ||||
| chr11:45180990-45181115 | Common:1; Rare:22 | ||||
| chr11:46274404-46274517 | Rare:16 | ||||
| chr11:46278485-46278602 | Rare:22 | ||||
| chr11:46312281-46312682 | Rare:109 | ||||
| chr11:46320200-46320745 | Common:8; Rare:145; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:47157596-47157879 | Common:3; Rare:62 | ||||
| chr11:47165445-47165548 | Common:8; Rare:44 | ||||
| chr11:47165726-47165877 | Rare:31 | ||||
| chr11:47172811-47172885 | Rare:12 | ||||
| chr11:47175913-47176204 | Common:1; Rare:83 | ||||
| chr11:47290044-47290296 | Rare:70 | ||||
| chr11:47359976-47360212 | Common:1; Rare:56 | ||||
| chr11:47376670-47376856 | Rare:37 |