| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128487874-128488059 | Common:1; Rare:48 | ||||
| chr3:128879408-128879669 | Common:4; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129160995-129161129 | Rare:54 | ||||
| chr3:129183758-129184119 | Common:2; Rare:135 | ||||
| chr3:129249524-129249683 | Common:2; Rare:49 | ||||
| chr3:129278761-129278892 | Common:4; Rare:43 | ||||
| chr3:129316245-129316289 | Rare:28 | ||||
| chr3:129439869-129440393 | Common:1; Rare:159; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129607191-129607230 | Rare:4 | ||||
| chr3:129893514-129893882 | Rare:139 | ||||
| chr3:130746785-130746853 | Rare:23 | ||||
| chr3:130850457-130850714 | Common:1; Rare:41 | ||||
| chr3:130893914-130894244 | Common:3; Rare:95 | ||||
| chr3:131026720-131026942 | Common:2; Rare:56 | ||||
| chr3:131381451-131381855 | Common:3; Rare:115 |