| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58499212-58499524 | Common:2; Rare:94; Clinvar:3 | ||||
| chr19:58519767-58520030 | Rare:70 | ||||
| chr19:58554939-58555344 | Common:2; Rare:134 | ||||
| chr2:677352-677518 | Common:1; Rare:66 | ||||
| chr2:1744457-1744625 | Common:1; Rare:60 | ||||
| chr2:3377811-3378069 | Common:2; Rare:80 | ||||
| chr2:3379608-3379761 | Common:1; Rare:62 | ||||
| chr2:3519492-3519636 | Common:2; Rare:46 | ||||
| chr2:3558251-3558658 | Common:6; Rare:150 | ||||
| chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9003957-9004076 | Rare:45 | ||||
| chr2:9423168-9423280 | Common:1; Rare:26 | ||||
| chr2:9423414-9423709 | Rare:94 | ||||
| chr2:9474500-9474630 | Common:6; Rare:62 | ||||
| chr2:9555730-9556052 | Common:2; Rare:107 |