| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22625721-22626115 | Common:3; Rare:124; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:22666709-22667102 | Common:1; Rare:109 | ||||
| chr11:22668105-22668151 | Rare:8 | ||||
| chr11:22668514-22668745 | Common:4; Rare:39 | ||||
| chr11:22672585-22672645 | Rare:13 | ||||
| chr11:22829262-22829447 | Common:1; Rare:53 | ||||
| chr11:22829710-22830082 | Common:4; Rare:131 | ||||
| chr11:27363083-27363466 | Rare:158 | ||||
| chr11:27506345-27506541 | Rare:46 | ||||
| chr11:27506691-27506987 | Common:1; Rare:121 | ||||
| chr11:28107821-28107896 | Rare:16 | ||||
| chr11:28108037-28108497 | Common:3; Rare:132 | ||||
| chr11:28110186-28110386 | Rare:52 | ||||
| chr11:30322840-30323221 | Common:4; Rare:101 | ||||
| chr11:30323261-30323446 | Common:2; Rare:56 |