| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111766342-111766433 | Common:1; Rare:54 | ||||
| chr11:111871296-111871344 | Rare:16 | ||||
| chr11:111878649-111879011 | Common:2; Rare:113 | ||||
| chr11:111879152-111879553 | Common:1; Rare:121 | ||||
| chr11:111937086-111937209 | Common:5; Rare:40 | ||||
| chr11:112025118-112025477 | Common:2; Rare:86; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:112073987-112074357 | Common:1; Rare:79 | ||||
| chr11:112086677-112086917 | Rare:107; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:112226314-112226446 | Rare:61 | ||||
| chr11:112226572-112226657 | Common:1; Rare:28 | ||||
| chr11:113314454-113314602 | Rare:51 | ||||
| chr11:113875485-113875815 | Common:4; Rare:123 | ||||
| chr11:114295501-114295877 | Common:3; Rare:63 | ||||
| chr11:114296255-114296549 | Rare:54 | ||||
| chr11:114400358-114400767 | Common:2; Rare:149 |