| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127590688-127590908 | Common:2; Rare:46 | ||||
| chr3:127598214-127598462 | Common:3; Rare:74 | ||||
| chr3:127672805-127673011 | Common:3; Rare:99 | ||||
| chr3:128052173-128052539 | Common:2; Rare:126 | ||||
| chr3:128153371-128153499 | Rare:37 | ||||
| chr3:128879391-128879682 | Common:4; Rare:139; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:129183831-129184084 | Common:2; Rare:87 | ||||
| chr3:129249524-129249744 | Common:2; Rare:62 | ||||
| chr3:129439754-129440364 | Common:1; Rare:184; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129560511-129560690 | Rare:45 | ||||
| chr3:129893545-129893882 | Rare:132 | ||||
| chr3:130746764-130746890 | Common:1; Rare:46 | ||||
| chr3:131026734-131026940 | Common:2; Rare:54 | ||||
| chr3:131381464-131381801 | Common:2; Rare:85 | ||||
| chr3:131502823-131503013 | Common:1; Rare:84 |