| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57257007-57257316 | Common:3; Rare:73 | ||||
| chr3:57577518-57577781 | Rare:40 | ||||
| chr3:57578365-57578527 | Common:2; Rare:27 | ||||
| chr3:57580554-57580659 | Rare:14 | ||||
| chr3:57583057-57583092 | Common:1; Rare:10 | ||||
| chr3:57583912-57584289 | Common:1; Rare:75 | ||||
| chr3:57584383-57584537 | Rare:32 | ||||
| chr3:57586479-57586668 | Common:1; Rare:33 | ||||
| chr3:57594165-57594430 | Rare:57 | ||||
| chr3:57616263-57616295 | Rare:5 | ||||
| chr3:57907923-57908080 | Rare:33; Clinvar:1 | ||||
| chr3:57952303-57952663 | Rare:58 | ||||
| chr3:58117493-58117858 | Common:2; Rare:69 | ||||
| chr3:58141605-58141895 | Rare:61; Clinvar:1 | ||||
| chr3:58163078-58163234 | Rare:46; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |