| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6481292-6481569 | Common:5; Rare:128 | ||||
| chr11:6603550-6603822 | Common:4; Rare:83; Clinvar (benign):3 | ||||
| chr11:6683234-6683480 | Common:5; Rare:116 | ||||
| chr11:8682644-8683036 | Common:2; Rare:162 | ||||
| chr11:8717883-8718184 | Common:7; Rare:79 | ||||
| chr11:8910935-8911270 | Common:6; Rare:91 | ||||
| chr11:8964366-8964558 | Common:4; Rare:62 | ||||
| chr11:8964919-8965020 | Common:1; Rare:26 | ||||
| chr11:9384527-9384680 | Common:1; Rare:56 | ||||
| chr11:9460670-9461010 | Common:4; Rare:89 | ||||
| chr11:9575464-9575790 | Common:1; Rare:58 | ||||
| chr11:10304804-10305150 | Common:1; Rare:79 | ||||
| chr11:10541145-10541312 | Rare:64 | ||||
| chr11:10750697-10751050 | Common:4; Rare:95 | ||||
| chr11:10751150-10751315 | Rare:50 |