| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:15035414-15035532 | Common:1; Rare:23 | ||||
| chr11:15053204-15053382 | Rare:30 | ||||
| chr11:15053591-15053991 | Common:1; Rare:81 | ||||
| chr11:15074600-15074990 | Common:3; Rare:91 | ||||
| chr11:15075010-15075290 | Rare:102 | ||||
| chr11:15106590-15106820 | Common:2; Rare:44 | ||||
| chr11:15106840-15107140 | Common:2; Rare:66 | ||||
| chr11:15258552-15258689 | Rare:13 | ||||
| chr11:15650107-15650360 | Common:2; Rare:48 | ||||
| chr11:15819642-15820042 | Common:2; Rare:119 | ||||
| chr11:15988880-15989260 | Rare:82; Clinvar (benign):1 | ||||
| chr11:16604805-16605233 | Common:8; Rare:189 | ||||
| chr11:16669820-16670260 | Common:3; Rare:76 | ||||
| chr11:16924704-16924965 | Common:1; Rare:54 | ||||
| chr11:17353373-17353505 | Rare:37 |