| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:31369735-31369887 | Rare:47 | ||||
| chr11:31509567-31509802 | Common:1; Rare:75 | ||||
| chr11:32435536-32435605 | Common:1; Rare:11 | ||||
| chr11:33161431-33161648 | Common:6; Rare:59 | ||||
| chr11:33257184-33257472 | Common:3; Rare:96 | ||||
| chr11:34438784-34439016 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr11:34620933-34621127 | Common:2; Rare:37 | ||||
| chr11:34624158-34624282 | Common:1; Rare:25 | ||||
| chr11:34916287-34916657 | Common:10; Rare:149; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138929-35139221 | Common:1; Rare:66 | ||||
| chr11:36289373-36289504 | Common:1; Rare:54 | ||||
| chr11:36510240-36510372 | Rare:37 | ||||
| chr11:43311788-43312053 | Common:2; Rare:85 | ||||
| chr11:43358844-43358988 | Rare:68 | ||||
| chr11:44066215-44066359 | Rare:28 |