| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118790888-118791255 | Rare:108 | ||||
| chr11:118997979-118998189 | Common:4; Rare:64 | ||||
| chr11:119018283-119018801 | Common:13; Rare:201 | ||||
| chr11:119057070-119057460 | Common:3; Rare:152 | ||||
| chr11:119067653-119067824 | Common:3; Rare:61 | ||||
| chr11:119206178-119206356 | Common:5; Rare:82; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:124673712-124673948 | Common:5; Rare:68 | ||||
| chr11:125111715-125111980 | Common:3; Rare:54 | ||||
| chr11:125592619-125592895 | Common:6; Rare:90 | ||||
| chr11:125625653-125626007 | Common:3; Rare:118 | ||||
| chr11:125887480-125887735 | Common:2; Rare:80 | ||||
| chr11:126211639-126211810 | Rare:78 | ||||
| chr11:126268534-126268649 | Common:2; Rare:29 | ||||
| chr11:126268779-126269209 | Common:2; Rare:166; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126355532-126355768 | Common:1; Rare:65 |