| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:747286-747565 | Rare:120; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:764178-764430 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:764724-764842 | Common:1; Rare:42; Clinvar:1 | ||||
| chr11:777451-777593 | Common:1; Rare:62 | ||||
| chr11:809492-809636 | Common:2; Rare:40 | ||||
| chr11:809640-810037 | Common:3; Rare:160 | ||||
| chr11:822214-822532 | Common:1; Rare:95; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr11:832839-833014 | Common:7; Rare:60 | ||||
| chr11:842456-842978 | Common:8; Rare:217 | ||||
| chr11:843964-844159 | Common:1; Rare:47 | ||||
| chr11:844195-844442 | Common:3; Rare:73 | ||||
| chr11:925567-926060 | Common:5; Rare:184 | ||||
| chr11:933413-933556 | Common:1; Rare:28 | ||||
| chr11:1309529-1309856 | Common:3; Rare:136 | ||||
| chr11:1839850-1840171 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):1 |