| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99727036-99727359 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:101612366-101612647 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:102449768-102449870 | Common:1; Rare:20 | ||||
| chr10:103659967-103660182 | Common:2; Rare:45 | ||||
| chr10:122113726-122113853 | Common:1; Rare:40 | ||||
| chr10:122155106-122155374 | Common:2; Rare:42 | ||||
| chr10:130110800-130110890 | Rare:27 | ||||
| chr10:130213418-130213527 | Rare:39 | ||||
| chr10:132065858-132066030 | Common:2; Rare:37 | ||||
| chr10:132575253-132575504 | Rare:33 | ||||
| chr10:133247532-133247691 | Common:2; Rare:46 | ||||
| chr11:322583-322743 | Common:2; Rare:20 | ||||
| chr11:1753474-1753869 | Common:3; Rare:163; Clinvar:10; Clinvar (benign):21; Clinvar (pathogenic):2 | ||||
| chr11:3477013-3477140 | Common:2; Rare:36 | ||||
| chr11:7906247-7906431 | Common:4; Rare:28 |