| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112164007-112164221 | Common:1; Rare:42 | ||||
| chr11:112226018-112226098 | Rare:8 | ||||
| chr11:112226218-112226461 | Rare:86 | ||||
| chr11:112226484-112226763 | Common:1; Rare:97; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112226785-112227035 | Rare:45 | ||||
| chr11:113314336-113314737 | Common:1; Rare:120 | ||||
| chr11:113314806-113314921 | Common:2; Rare:44 | ||||
| chr11:113387872-113387995 | Rare:42 | ||||
| chr11:113475396-113475416 | Rare:3 | ||||
| chr11:113773190-113773315 | Common:1; Rare:20 | ||||
| chr11:113773479-113773526 | Rare:15 | ||||
| chr11:113773618-113773911 | Common:1; Rare:87 | ||||
| chr11:113875248-113875304 | Rare:9 | ||||
| chr11:113875450-113875905 | Common:4; Rare:167 | ||||
| chr11:113876004-113876069 | Rare:14 |