| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:93741493-93741693 | Common:4; Rare:72 | ||||
| chr11:94493800-94494003 | Common:3; Rare:58; Clinvar (benign):1 | ||||
| chr11:94973542-94973841 | Rare:76 | ||||
| chr11:95790378-95790562 | Rare:70 | ||||
| chr11:102452674-102452900 | Rare:70 | ||||
| chr11:106077348-106077682 | Common:2; Rare:92 | ||||
| chr11:111913142-111913278 | Rare:41 | ||||
| chr11:112074175-112074343 | Common:1; Rare:39 | ||||
| chr11:112086731-112086899 | Rare:67 | ||||
| chr11:118997983-118998148 | Common:4; Rare:43 | ||||
| chr11:119067660-119067816 | Common:2; Rare:56 | ||||
| chr11:124673695-124673916 | Common:4; Rare:71 | ||||
| chr11:125887480-125887727 | Common:2; Rare:78 | ||||
| chr11:126268848-126269184 | Common:1; Rare:119; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126303983-126304083 | Rare:57 |