| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118135995-118136175 | Common:2; Rare:49 | ||||
| chr12:120201085-120201311 | Common:2; Rare:74 | ||||
| chr12:120446359-120446478 | Common:1; Rare:53 | ||||
| chr12:120469575-120469889 | Common:3; Rare:110 | ||||
| chr12:120495907-120496158 | Common:5; Rare:79 | ||||
| chr12:122526921-122527260 | Common:3; Rare:101 | ||||
| chr12:123233121-123233458 | Common:2; Rare:105; Clinvar:1 | ||||
| chr12:123364803-123364964 | Common:2; Rare:63 | ||||
| chr12:123633640-123633860 | Common:1; Rare:99; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:132887573-132887798 | Rare:60 | ||||
| chr13:21176545-21176704 | Common:1; Rare:79 | ||||
| chr13:25301500-25301706 | Common:1; Rare:80 | ||||
| chr13:28658942-28659175 | Rare:101; Clinvar (pathogenic):1 | ||||
| chr13:30307001-30307224 | Common:4; Rare:59 | ||||
| chr13:33285677-33285902 | Rare:50 |