| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:4094737-4094877 | Common:1; Rare:42 | ||||
| chr11:4393654-4393779 | Rare:26 | ||||
| chr11:5624915-5625029 | Rare:17 | ||||
| chr11:6320127-6320272 | Common:2; Rare:57 | ||||
| chr11:6390237-6390562 | Common:3; Rare:98; Clinvar (benign):1 | ||||
| chr11:6481304-6481530 | Common:4; Rare:94 | ||||
| chr11:6603550-6603831 | Common:4; Rare:85; Clinvar (benign):3 | ||||
| chr11:6619382-6619570 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):8 | ||||
| chr11:7020327-7020476 | Rare:49 | ||||
| chr11:7485265-7485498 | Rare:38 | ||||
| chr11:7513626-7513948 | Common:5; Rare:93 | ||||
| chr11:8168985-8169095 | Common:2; Rare:37 | ||||
| chr11:8682650-8682816 | Common:2; Rare:74 | ||||
| chr11:8964366-8964531 | Common:4; Rare:53 | ||||
| chr11:8964919-8965061 | Common:2; Rare:38 |