| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6473871-6474100 | Rare:77 | ||||
| chr11:6481299-6481539 | Common:4; Rare:103 | ||||
| chr11:6603536-6603860 | Common:4; Rare:97; Clinvar (benign):3 | ||||
| chr11:6683241-6683425 | Common:3; Rare:91 | ||||
| chr11:8682650-8682820 | Common:2; Rare:74 | ||||
| chr11:8964370-8964497 | Common:2; Rare:40 | ||||
| chr11:8964919-8965020 | Common:1; Rare:26 | ||||
| chr11:9314572-9314917 | Common:4; Rare:106 | ||||
| chr11:9460696-9461048 | Common:3; Rare:98 | ||||
| chr11:10304840-10305118 | Common:1; Rare:67 | ||||
| chr11:10541145-10541312 | Rare:64 | ||||
| chr11:10568614-10568931 | Common:1; Rare:53 | ||||
| chr11:10751188-10751285 | Rare:30 | ||||
| chr11:10808874-10809117 | Common:1; Rare:104 | ||||
| chr11:10858023-10858279 | Common:2; Rare:82 |