| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:11621984-11622222 | Common:3; Rare:93 | ||||
| chr11:11841914-11842079 | Common:1; Rare:46 | ||||
| chr11:12008548-12008726 | Common:2; Rare:45 | ||||
| chr11:13009134-13009322 | Common:1; Rare:69 | ||||
| chr11:13463153-13463340 | Common:1; Rare:67 | ||||
| chr11:13668342-13668759 | Common:1; Rare:134 | ||||
| chr11:14499782-14499918 | Common:2; Rare:47 | ||||
| chr11:14891641-14891779 | Rare:37 | ||||
| chr11:16607737-16608105 | Common:1; Rare:68 | ||||
| chr11:16738436-16738729 | Common:3; Rare:67 | ||||
| chr11:17077595-17077910 | Common:2; Rare:133 | ||||
| chr11:17207920-17208098 | Common:1; Rare:68 | ||||
| chr11:17276541-17276823 | Common:5; Rare:81; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18012925-18013248 | Common:6; Rare:108 | ||||
| chr11:18322131-18322306 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):2 |