| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47185689-47186097 | Common:2; Rare:154 | ||||
| chr11:47186262-47186662 | Rare:187 | ||||
| chr11:47214708-47215125 | Common:7; Rare:244; Clinvar:6; Clinvar (benign):2 | ||||
| chr11:47215145-47215770 | Rare:234 | ||||
| chr11:47248132-47248532 | Common:2; Rare:101 | ||||
| chr11:47248577-47249320 | Common:7; Rare:748; Clinvar (benign):3 | ||||
| chr11:47257658-47258301 | Common:1; Rare:262 | ||||
| chr11:47268860-47269440 | Common:9; Rare:420 | ||||
| chr11:47269390-47269860 | Common:9; Rare:566 | ||||
| chr11:47269883-47270313 | Common:14; Rare:843 | ||||
| chr11:47270322-47270722 | Common:2; Rare:67 | ||||
| chr11:47271992-47272401 | Common:14; Rare:214 | ||||
| chr11:47378325-47378785 | Common:1; Rare:465 | ||||
| chr11:47406902-47407719 | Common:8; Rare:351 | ||||
| chr11:47407940-47408736 | Common:11; Rare:794; Clinvar:1; Clinvar (benign):5 |