| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67436250-67436753 | Common:2; Rare:127 | ||||
| chr11:67437050-67437371 | Common:1; Rare:87 | ||||
| chr11:67438592-67438849 | Common:4; Rare:100 | ||||
| chr11:67444978-67445165 | Rare:37 | ||||
| chr11:67460072-67460180 | Common:1; Rare:22; Clinvar (benign):1 | ||||
| chr11:67460348-67460377 | Common:1; Rare:4; Clinvar (benign):1 | ||||
| chr11:67483910-67484095 | Common:1; Rare:30 | ||||
| chr11:67484473-67484517 | Rare:9 | ||||
| chr11:67485096-67485268 | Rare:31 | ||||
| chr11:67485883-67486079 | Rare:29 | ||||
| chr11:67486091-67486196 | Common:1; Rare:17 | ||||
| chr11:67486800-67486951 | Rare:34 | ||||
| chr11:67558014-67558350 | Common:1; Rare:57 | ||||
| chr11:67562034-67562062 | Rare:3 | ||||
| chr11:67562094-67562158 | Rare:11 |