| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66051930-66052456 | Common:9; Rare:163 | ||||
| chr11:66070009-66070093 | Rare:22 | ||||
| chr11:66070185-66070410 | Common:1; Rare:75 | ||||
| chr11:66100761-66100786 | Rare:5 | ||||
| chr11:66100896-66100992 | Common:1; Rare:20 | ||||
| chr11:66257087-66257393 | Common:2; Rare:51 | ||||
| chr11:66257473-66257683 | Rare:52 | ||||
| chr11:66258342-66258513 | Rare:38 | ||||
| chr11:66267981-66268061 | Rare:16 | ||||
| chr11:66268294-66268706 | Common:3; Rare:114 | ||||
| chr11:66268763-66268937 | Common:2; Rare:52 | ||||
| chr11:66289016-66289481 | Common:1; Rare:117 | ||||
| chr11:66289630-66289813 | Common:1; Rare:41 | ||||
| chr11:66344988-66345293 | Common:1; Rare:82 | ||||
| chr11:66347556-66347891 | Common:5; Rare:84; Clinvar (benign):2 |