| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94544029-94544467 | Common:3; Rare:184 | ||||
| chr11:94973492-94973874 | Rare:105 | ||||
| chr11:95066784-95066960 | Rare:31 | ||||
| chr11:95067087-95067258 | Rare:56 | ||||
| chr11:95067364-95067611 | Common:1; Rare:99 | ||||
| chr11:95089424-95089496 | Common:2; Rare:17 | ||||
| chr11:95089588-95089931 | Common:4; Rare:122 | ||||
| chr11:95231194-95231650 | Common:2; Rare:131 | ||||
| chr11:95232303-95232496 | Rare:35 | ||||
| chr11:95788748-95789127 | Common:2; Rare:120 | ||||
| chr11:95789380-95790257 | Common:6; Rare:335 | ||||
| chr11:95790319-95790754 | Common:3; Rare:179; Clinvar:2 | ||||
| chr11:95790891-95790947 | Common:1; Rare:11 | ||||
| chr11:95791109-95791225 | Rare:42 | ||||
| chr11:95923794-95924232 | Common:2; Rare:180; Clinvar:6; Clinvar (benign):5 |