| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127823169-127823313 | Common:3; Rare:28 | ||||
| chr3:128052196-128052492 | Common:2; Rare:97 | ||||
| chr3:128123725-128123961 | Rare:72 | ||||
| chr3:128153383-128153493 | Rare:32 | ||||
| chr3:128487878-128488107 | Common:1; Rare:64 | ||||
| chr3:128650775-128651164 | Common:2; Rare:106 | ||||
| chr3:128726056-128726189 | Common:1; Rare:32; Clinvar:2 | ||||
| chr3:128879394-128879671 | Common:4; Rare:132; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183794-129184079 | Common:2; Rare:95 | ||||
| chr3:129249558-129249683 | Common:1; Rare:37 | ||||
| chr3:129278743-129278892 | Common:4; Rare:45 | ||||
| chr3:129316283-129316360 | Common:1; Rare:25 | ||||
| chr3:129439847-129440247 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129560522-129560680 | Rare:41 | ||||
| chr3:129893571-129893882 | Rare:130 |