| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16395116-16395332 | Common:1; Rare:36 | ||||
| chr11:16614262-16614381 | Rare:24 | ||||
| chr11:16922925-16923046 | Common:1; Rare:16 | ||||
| chr11:17215804-17215932 | Common:1; Rare:23 | ||||
| chr11:17353627-17353773 | Common:5; Rare:47 | ||||
| chr11:17696926-17697074 | Common:1; Rare:31 | ||||
| chr11:17883772-17884002 | Common:4; Rare:45 | ||||
| chr11:18209104-18209237 | Common:5; Rare:37 | ||||
| chr11:18310849-18311041 | Rare:67; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:18323323-18323404 | Common:1; Rare:18 | ||||
| chr11:19135458-19135714 | Common:1; Rare:69 | ||||
| chr11:19262333-19262415 | Rare:16 | ||||
| chr11:19505745-19506009 | Common:3; Rare:42 | ||||
| chr11:20122464-20122608 | Common:3; Rare:22 | ||||
| chr11:20596964-20597141 | Common:3; Rare:47 |