| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65503962-65504357 | Common:2; Rare:196 | ||||
| chr11:65540652-65540813 | Common:3; Rare:57 | ||||
| chr11:65546564-65546837 | Common:3; Rare:91; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65570286-65570513 | Rare:85 | ||||
| chr11:65575844-65576036 | Common:3; Rare:55 | ||||
| chr11:65614240-65614335 | Rare:20 | ||||
| chr11:65637996-65638147 | Common:3; Rare:69 | ||||
| chr11:65639695-65639927 | Rare:43 | ||||
| chr11:65640272-65640484 | Common:1; Rare:39 | ||||
| chr11:65662902-65663017 | Common:1; Rare:30 | ||||
| chr11:65663096-65663335 | Common:3; Rare:57 | ||||
| chr11:65856995-65857334 | Common:4; Rare:101 | ||||
| chr11:65860297-65860476 | Common:2; Rare:63 | ||||
| chr11:65873570-65873749 | Common:2; Rare:63 | ||||
| chr11:65888441-65888707 | Common:1; Rare:84 |