| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:133452683-133453040 | Common:3; Rare:81 | ||||
| chr3:133452950-133453470 | Common:2; Rare:73 | ||||
| chr3:133453807-133454123 | Common:4; Rare:53 | ||||
| chr3:133455006-133455350 | Common:2; Rare:63 | ||||
| chr3:133455987-133456410 | Rare:82 | ||||
| chr3:133456989-133457389 | Common:2; Rare:123 | ||||
| chr3:133459251-133459638 | Common:3; Rare:120 | ||||
| chr3:133460410-133460622 | Rare:41 | ||||
| chr3:133460834-133461058 | Rare:64 | ||||
| chr3:133461200-133461849 | Common:11; Rare:191 | ||||
| chr3:133462046-133462282 | Common:5; Rare:32 | ||||
| chr3:133463434-133464030 | Common:3; Rare:161 | ||||
| chr3:133474155-133474607 | Common:14; Rare:182 | ||||
| chr3:133475134-133475426 | Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:133488950-133489290 | Common:3; Rare:85 |