| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111923738-111924037 | Common:2; Rare:48 | ||||
| chr11:111937092-111937209 | Common:5; Rare:39 | ||||
| chr11:112024957-112025195 | Rare:58; Clinvar:3 | ||||
| chr11:112025327-112025632 | Common:2; Rare:96; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:112073995-112074412 | Common:1; Rare:85 | ||||
| chr11:112086703-112086917 | Rare:93; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:112226238-112226699 | Common:1; Rare:174; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961164-112961532 | Common:1; Rare:148 | ||||
| chr11:113314448-113314602 | Rare:54 | ||||
| chr11:113314787-113314870 | Common:1; Rare:25 | ||||
| chr11:113773646-113773842 | Common:1; Rare:63 | ||||
| chr11:113875485-113875819 | Common:4; Rare:126 | ||||
| chr11:114400400-114400784 | Common:2; Rare:143 | ||||
| chr11:114439311-114439645 | Common:3; Rare:111 | ||||
| chr11:116772957-116773088 | Rare:47 |