| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16738456-16738734 | Common:3; Rare:60 | ||||
| chr11:17077430-17077765 | Common:4; Rare:127 | ||||
| chr11:17207922-17208089 | Common:1; Rare:65 | ||||
| chr11:17276479-17276827 | Common:5; Rare:101; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18012896-18013251 | Common:6; Rare:119 | ||||
| chr11:18106037-18106308 | Common:2; Rare:83 | ||||
| chr11:18322131-18322321 | Common:4; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322491-18322631 | Common:2; Rare:62 | ||||
| chr11:18394272-18394630 | Common:1; Rare:129; Clinvar (benign):1 | ||||
| chr11:18526812-18526971 | Rare:74 | ||||
| chr11:18588672-18588884 | Common:2; Rare:71 | ||||
| chr11:18634332-18634574 | Common:2; Rare:77 | ||||
| chr11:20363683-20363783 | Common:2; Rare:24 | ||||
| chr11:20387417-20387765 | Common:7; Rare:113 | ||||
| chr11:22625817-22626002 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 |