| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47268984-47269395 | Common:1; Rare:79 | ||||
| chr11:47269400-47269831 | Common:3; Rare:134 | ||||
| chr11:47269906-47270227 | Common:2; Rare:110 | ||||
| chr11:47407999-47408247 | Rare:45 | ||||
| chr11:47408281-47408726 | Common:4; Rare:127; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:47408731-47408844 | Rare:14 | ||||
| chr11:47408873-47408934 | Common:1; Rare:14 | ||||
| chr11:47408958-47409329 | Common:1; Rare:71 | ||||
| chr11:47409744-47409901 | Common:1; Rare:29 | ||||
| chr11:47426170-47426297 | Rare:46 | ||||
| chr11:47426363-47426671 | Common:1; Rare:77 | ||||
| chr11:47426916-47426983 | Common:1; Rare:15 | ||||
| chr11:47523647-47523834 | Common:1; Rare:26 | ||||
| chr11:47552649-47552816 | Common:1; Rare:74 | ||||
| chr11:47552821-47552970 | Common:1; Rare:52 |