| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6604059-6604069 | Rare:3 | ||||
| chr11:6611983-6612288 | Common:1; Rare:107 | ||||
| chr11:6619405-6619566 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:6683261-6683652 | Common:6; Rare:148 | ||||
| chr11:6926411-6926562 | Common:4; Rare:48 | ||||
| chr11:7020305-7020462 | Rare:50 | ||||
| chr11:7513638-7513972 | Common:5; Rare:99 | ||||
| chr11:8594184-8594327 | Rare:49 | ||||
| chr11:8682599-8683046 | Common:2; Rare:188 | ||||
| chr11:8910935-8911235 | Common:6; Rare:85 | ||||
| chr11:8964366-8964564 | Common:4; Rare:65 | ||||
| chr11:8964896-8965020 | Common:2; Rare:34 | ||||
| chr11:9314557-9314950 | Common:4; Rare:115 | ||||
| chr11:9384335-9384712 | Common:3; Rare:108 | ||||
| chr11:9460601-9461050 | Common:4; Rare:114 |