| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14520275-14520545 | Rare:93 | ||||
| chr11:14643591-14643810 | Common:2; Rare:82 | ||||
| chr11:14891511-14891712 | Common:1; Rare:61 | ||||
| chr11:15114816-15114966 | Common:3; Rare:49 | ||||
| chr11:16607810-16607894 | Rare:13 | ||||
| chr11:16738430-16738781 | Common:3; Rare:83 | ||||
| chr11:17013788-17013994 | Common:6; Rare:70 | ||||
| chr11:17014130-17014335 | Common:1; Rare:79 | ||||
| chr11:17076127-17076449 | Common:4; Rare:71 | ||||
| chr11:17077607-17077868 | Common:2; Rare:108 | ||||
| chr11:17207856-17208111 | Common:2; Rare:91 | ||||
| chr11:17276475-17276823 | Common:5; Rare:102; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17476803-17476931 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18012903-18013254 | Common:6; Rare:117 | ||||
| chr11:18322107-18322328 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):2 |