| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9137621-9138021 | Common:4; Rare:109 | ||||
| chr11:9264708-9265108 | Common:2; Rare:198 | ||||
| chr11:9265256-9265494 | Common:2; Rare:187 | ||||
| chr11:9314453-9315009 | Common:15; Rare:375 | ||||
| chr11:9384499-9384755 | Common:3; Rare:232 | ||||
| chr11:9460549-9461199 | Common:12; Rare:414 | ||||
| chr11:9461234-9461498 | Common:11; Rare:228 | ||||
| chr11:9572981-9573991 | Common:16; Rare:690 | ||||
| chr11:9574557-9574728 | Rare:67 | ||||
| chr11:9575101-9575253 | Rare:75 | ||||
| chr11:9575341-9575813 | Common:3; Rare:109 | ||||
| chr11:9663923-9664252 | Common:11; Rare:248 | ||||
| chr11:9719517-9720126 | Common:5; Rare:214 | ||||
| chr11:10293731-10294131 | Common:6; Rare:137; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:10294032-10294320 | Common:3; Rare:146; Clinvar:9; Clinvar (pathogenic):2 |