| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126268800-126269207 | Common:2; Rare:159; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126283002-126283078 | Common:1; Rare:22 | ||||
| chr11:126303959-126304104 | Rare:83 | ||||
| chr11:126355532-126355760 | Common:1; Rare:62 | ||||
| chr11:129279500-129279731 | Common:3; Rare:98 | ||||
| chr11:129815712-129815877 | Common:1; Rare:39 | ||||
| chr11:129895516-129895687 | Common:2; Rare:68 | ||||
| chr11:130069624-130070080 | Common:2; Rare:162 | ||||
| chr11:130314389-130314495 | Common:1; Rare:31 | ||||
| chr11:130314785-130315040 | Common:4; Rare:91 | ||||
| chr11:130448327-130448645 | Rare:75 | ||||
| chr11:130916415-130916676 | Common:5; Rare:81 | ||||
| chr11:131911303-131911484 | Common:1; Rare:68 | ||||
| chr11:133532315-133532417 | Rare:28 | ||||
| chr11:133532476-133532527 | Rare:6 |