| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46295610-46295830 | Rare:52 | ||||
| chr11:46315811-46316130 | Common:3; Rare:50 | ||||
| chr11:46347219-46347574 | Common:4; Rare:217 | ||||
| chr11:46593962-46594195 | Common:3; Rare:89 | ||||
| chr11:46617144-46617607 | Common:10; Rare:259 | ||||
| chr11:46700515-46700818 | Common:2; Rare:121 | ||||
| chr11:46701004-46701106 | Common:2; Rare:73 | ||||
| chr11:46846149-46846422 | Common:2; Rare:147 | ||||
| chr11:46918527-46918690 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:46936641-46936818 | Common:4; Rare:103 | ||||
| chr11:47176837-47177152 | Common:1; Rare:229 | ||||
| chr11:47185290-47185750 | Common:4; Rare:151 | ||||
| chr11:47186352-47186551 | Rare:109 | ||||
| chr11:47214314-47214677 | Common:3; Rare:85 | ||||
| chr11:47214809-47215134 | Common:4; Rare:170; Clinvar:6; Clinvar (benign):2 |