| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6234612-6234871 | Common:2; Rare:80 | ||||
| chr11:6320490-6320568 | Common:2; Rare:25 | ||||
| chr11:6390322-6390567 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr11:6481274-6481525 | Common:4; Rare:97 | ||||
| chr11:6603553-6603831 | Common:4; Rare:85; Clinvar (benign):3 | ||||
| chr11:6614929-6615264 | Common:1; Rare:90; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):4 | ||||
| chr11:6683234-6683644 | Common:6; Rare:157 | ||||
| chr11:7513632-7513948 | Common:5; Rare:91 | ||||
| chr11:8168991-8169062 | Common:1; Rare:27 | ||||
| chr11:8682650-8682820 | Common:2; Rare:74 | ||||
| chr11:8717935-8718184 | Common:7; Rare:59 | ||||
| chr11:8910942-8911256 | Common:5; Rare:89 | ||||
| chr11:8964361-8964519 | Common:4; Rare:58 | ||||
| chr11:8964738-8964887 | Rare:34 | ||||
| chr11:8964932-8964982 | Common:1; Rare:9 |