| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118925870-118926138 | Common:2; Rare:78 | ||||
| chr11:118997980-118998193 | Common:4; Rare:66 | ||||
| chr11:119017582-119018513 | Common:12; Rare:317 | ||||
| chr11:119018574-119018813 | Common:5; Rare:88 | ||||
| chr11:119047808-119048026 | Common:1; Rare:79 | ||||
| chr11:119057064-119057481 | Common:3; Rare:161 | ||||
| chr11:119067632-119067840 | Common:3; Rare:70 | ||||
| chr11:119101374-119101572 | Rare:58; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:119206180-119206432 | Common:5; Rare:109; Clinvar:8; Clinvar (benign):6 | ||||
| chr11:119381557-119381836 | Common:1; Rare:73 | ||||
| chr11:119729140-119729587 | Common:2; Rare:117 | ||||
| chr11:120123184-120123195 | Common:1; Rare:1 | ||||
| chr11:120125866-120126204 | Common:1; Rare:74 | ||||
| chr11:120128666-120129049 | Common:2; Rare:86 | ||||
| chr11:120137975-120138451 | Common:3; Rare:126 |