| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9460682-9461050 | Common:4; Rare:98 | ||||
| chr11:9663919-9664237 | Common:4; Rare:111 | ||||
| chr11:10456227-10456319 | Rare:21 | ||||
| chr11:10541145-10541345 | Rare:74 | ||||
| chr11:10751172-10751302 | Rare:40 | ||||
| chr11:10808877-10808987 | Common:1; Rare:55 | ||||
| chr11:10858013-10858310 | Common:3; Rare:95 | ||||
| chr11:11841809-11842056 | Common:3; Rare:89 | ||||
| chr11:13463147-13463395 | Common:1; Rare:92 | ||||
| chr11:14520318-14520457 | Rare:40 | ||||
| chr11:14891646-14891789 | Rare:36 | ||||
| chr11:16738466-16738707 | Common:3; Rare:52 | ||||
| chr11:17207910-17208126 | Common:2; Rare:84 | ||||
| chr11:17276450-17276813 | Common:4; Rare:104; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18322113-18322300 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):2 |