| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45163674-45164008 | Common:4; Rare:121 | ||||
| chr22:46250254-46250408 | Common:2; Rare:47 | ||||
| chr22:46296655-46296918 | Common:2; Rare:93 | ||||
| chr22:46335619-46335760 | Common:2; Rare:58; Clinvar:4; Clinvar (benign):6 | ||||
| chr22:46762520-46762706 | Common:3; Rare:66 | ||||
| chr22:50487012-50487187 | Rare:50 | ||||
| chr22:50582818-50583121 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50783601-50783876 | Common:2; Rare:85 | ||||
| chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 | ||||
| chr3:4493180-4493483 | Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:9362989-9363134 | Rare:50 | ||||
| chr3:9792382-9792521 | Rare:41 | ||||
| chr3:9792732-9793123 | Common:3; Rare:135 | ||||
| chr3:9843975-9844137 | Common:2; Rare:65 | ||||
| chr3:9933546-9933857 | Common:2; Rare:124; Clinvar:2 |