| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:128715680-128715686 | Rare:1 | ||||
| chr11:129861880-129861938 | Rare:12 | ||||
| chr11:130427771-130427856 | Common:1; Rare:32 | ||||
| chr11:130914267-130914316 | Rare:11 | ||||
| chr11:131256378-131256679 | Common:13; Rare:48 | ||||
| chr11:131391404-131391623 | Common:2; Rare:32 | ||||
| chr12:16721-16847 | Common:4; Rare:42 | ||||
| chr12:753767-754319 | Common:4; Rare:175; Clinvar:11; Clinvar (benign):8 | ||||
| chr12:926521-926798 | Common:3; Rare:51 | ||||
| chr12:2797441-2797781 | Common:1; Rare:80 | ||||
| chr12:2800169-2800577 | Common:1; Rare:86 | ||||
| chr12:2878087-2878361 | Common:1; Rare:46 | ||||
| chr12:4012819-4012983 | Common:1; Rare:31 | ||||
| chr12:6160137-6160304 | Common:4; Rare:38 | ||||
| chr12:6202247-6202506 | Rare:51 |