| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108222561-108223128 | Common:1; Rare:187; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108223249-108223441 | Rare:52 | ||||
| chr11:108467484-108467642 | Common:3; Rare:65 | ||||
| chr11:110296472-110296788 | Common:1; Rare:145; Clinvar:9 | ||||
| chr11:110430033-110430272 | Common:4; Rare:56 | ||||
| chr11:111602168-111602481 | Common:1; Rare:103 | ||||
| chr11:111766344-111766426 | Rare:43 | ||||
| chr11:111871254-111871391 | Rare:42; Clinvar:1 | ||||
| chr11:111878827-111879016 | Common:2; Rare:71 | ||||
| chr11:111879030-111879548 | Common:2; Rare:181 | ||||
| chr11:111912052-111912220 | Common:2; Rare:26 | ||||
| chr11:111912708-111912796 | Rare:10 | ||||
| chr11:111926967-111927273 | Common:9; Rare:57 | ||||
| chr11:111937105-111937439 | Common:7; Rare:97 | ||||
| chr11:111977069-111977395 | Common:4; Rare:72 |