| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:21015392-21016120 | Common:5; Rare:153; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:21018100-21018712 | Common:6; Rare:157 | ||||
| chr2:21019863-21020300 | Rare:145; Clinvar:1; Clinvar (benign):6 | ||||
| chr2:21026820-21027429 | Common:3; Rare:162; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:21031877-21032873 | Common:6; Rare:245; Clinvar:10; Clinvar (benign):7 | ||||
| chr2:21034730-21035280 | Common:3; Rare:110; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:21037840-21038310 | Common:4; Rare:217; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr2:21055480-21055860 | Common:1; Rare:67 | ||||
| chr2:21067062-21067950 | Common:18; Rare:314 | ||||
| chr2:21070337-21070582 | Common:5; Rare:79 | ||||
| chr2:21070630-21071063 | Common:3; Rare:174 | ||||
| chr2:25997692-25998092 | Common:21; Rare:220 | ||||
| chr2:27095353-27096051 | Common:3; Rare:194 | ||||
| chr2:27177570-27178050 | Common:3; Rare:151 | ||||
| chr2:27180445-27181119 | Common:4; Rare:202 |