| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:13440047-13440310 | Rare:55 | ||||
| chr11:13463141-13463367 | Common:1; Rare:82 | ||||
| chr11:14499773-14499959 | Common:3; Rare:61 | ||||
| chr11:14520256-14520549 | Rare:98 | ||||
| chr11:14643619-14643765 | Common:1; Rare:67 | ||||
| chr11:14644642-14644859 | Rare:96 | ||||
| chr11:14891610-14891738 | Rare:42 | ||||
| chr11:16605958-16606150 | Common:1; Rare:43 | ||||
| chr11:16607512-16607590 | Rare:25 | ||||
| chr11:16607658-16607877 | Common:1; Rare:31 | ||||
| chr11:16738432-16738842 | Common:3; Rare:101 | ||||
| chr11:17077595-17077934 | Common:2; Rare:140 | ||||
| chr11:17207919-17208111 | Common:1; Rare:72 | ||||
| chr11:17276475-17276818 | Common:4; Rare:102; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17351530-17351834 | Common:1; Rare:62 |