| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8964409-8964531 | Common:3; Rare:34 | ||||
| chr11:9314562-9314920 | Common:4; Rare:111 | ||||
| chr11:9460627-9460956 | Common:3; Rare:84 | ||||
| chr11:9663995-9664169 | Common:4; Rare:61 | ||||
| chr11:10304907-10305088 | Common:1; Rare:40 | ||||
| chr11:10541150-10541282 | Rare:44 | ||||
| chr11:10751183-10751279 | Rare:30 | ||||
| chr11:10858023-10858246 | Common:2; Rare:68 | ||||
| chr11:13463168-13463326 | Rare:61 | ||||
| chr11:14520318-14520597 | Rare:86 | ||||
| chr11:16738441-16738717 | Common:3; Rare:62 | ||||
| chr11:17077572-17077852 | Common:3; Rare:124 | ||||
| chr11:17207920-17208059 | Common:1; Rare:55 | ||||
| chr11:17276544-17276809 | Common:4; Rare:74; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18322130-18322302 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):2 |