| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17014723-17015440 | Common:2; Rare:202 | ||||
| chr11:17077515-17077990 | Common:8; Rare:463 | ||||
| chr11:17207861-17208201 | Common:6; Rare:293 | ||||
| chr11:17208359-17208642 | Rare:89 | ||||
| chr11:17276148-17276340 | Common:3; Rare:75 | ||||
| chr11:17276376-17276831 | Common:14; Rare:304; Clinvar:11; Clinvar (pathogenic):3 | ||||
| chr11:17351586-17351812 | Common:1; Rare:51 | ||||
| chr11:17387887-17388930 | Common:5; Rare:282; Clinvar:14; Clinvar (benign):7; Clinvar (pathogenic):7 | ||||
| chr11:17389040-17389850 | Common:10; Rare:296 | ||||
| chr11:17413590-17413940 | Common:1; Rare:98 | ||||
| chr11:17476320-17476676 | Common:3; Rare:171; Clinvar:2 | ||||
| chr11:17544264-17544664 | Common:11; Rare:178; Clinvar:5 | ||||
| chr11:18012886-18013306 | Common:16; Rare:296 | ||||
| chr11:18322032-18322648 | Common:25; Rare:580; Clinvar:6; Clinvar (benign):7 | ||||
| chr11:18394315-18394744 | Common:3; Rare:352; Clinvar (benign):3 |