| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:11841849-11842079 | Common:3; Rare:75 | ||||
| chr11:12110354-12110649 | Rare:73 | ||||
| chr11:12207485-12207651 | Common:1; Rare:34 | ||||
| chr11:12224598-12224765 | Common:2; Rare:51 | ||||
| chr11:12377422-12377643 | Rare:86 | ||||
| chr11:13463141-13463403 | Common:1; Rare:98 | ||||
| chr11:14499771-14499962 | Common:3; Rare:63 | ||||
| chr11:14520275-14520555 | Rare:95 | ||||
| chr11:16738432-16738729 | Common:3; Rare:68 | ||||
| chr11:17077564-17077921 | Common:3; Rare:155 | ||||
| chr11:17207910-17208102 | Common:2; Rare:73 | ||||
| chr11:17276465-17276816 | Common:4; Rare:102; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18012896-18013246 | Common:6; Rare:117 | ||||
| chr11:18105998-18106308 | Common:3; Rare:107 | ||||
| chr11:18322108-18322321 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):2 |