| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:12008584-12008718 | Common:1; Rare:35 | ||||
| chr11:12377459-12377738 | Rare:105 | ||||
| chr11:12473815-12473983 | Rare:51 | ||||
| chr11:12675269-12675496 | Rare:76 | ||||
| chr11:13463159-13463341 | Common:1; Rare:65 | ||||
| chr11:13962502-13962892 | Common:3; Rare:95 | ||||
| chr11:14520314-14520498 | Rare:56 | ||||
| chr11:14643619-14643942 | Common:1; Rare:114 | ||||
| chr11:14891646-14891813 | Rare:44 | ||||
| chr11:14892176-14892267 | Rare:45 | ||||
| chr11:16738450-16738791 | Common:3; Rare:77 | ||||
| chr11:17077595-17077847 | Common:2; Rare:103 | ||||
| chr11:17207910-17208089 | Common:2; Rare:71 | ||||
| chr11:17276451-17276806 | Common:4; Rare:101; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18106045-18106308 | Common:2; Rare:75 |