| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18394331-18394778 | Common:3; Rare:159; Clinvar (benign):1 | ||||
| chr11:18396028-18396431 | Common:2; Rare:128 | ||||
| chr11:18526330-18526780 | Common:3; Rare:111 | ||||
| chr11:18526851-18527011 | Common:1; Rare:78 | ||||
| chr11:18588621-18588863 | Common:2; Rare:88 | ||||
| chr11:18634319-18634630 | Common:3; Rare:106 | ||||
| chr11:18634759-18634906 | Common:2; Rare:40 | ||||
| chr11:18698515-18698803 | Common:6; Rare:72 | ||||
| chr11:19116953-19117227 | Common:3; Rare:76 | ||||
| chr11:19240847-19241178 | Rare:100 | ||||
| chr11:19241612-19241750 | Rare:36 | ||||
| chr11:19712640-19712843 | Common:2; Rare:76 | ||||
| chr11:20363656-20363824 | Common:3; Rare:34 | ||||
| chr11:20364040-20364171 | Common:6; Rare:29 | ||||
| chr11:20387379-20387749 | Common:8; Rare:121 |