| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:154590627-154590986 | Common:3; Rare:83; Clinvar (benign):3 | ||||
| chr4:154612339-154612964 | Common:1; Rare:157; Clinvar:3 | ||||
| chr4:158671825-158672489 | Common:5; Rare:184; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:158723202-158723497 | Common:2; Rare:128 | ||||
| chr4:159103958-159104175 | Common:1; Rare:80 | ||||
| chr4:163166826-163166957 | Common:2; Rare:41 | ||||
| chr4:165112786-165113015 | Common:1; Rare:75 | ||||
| chr4:165327411-165327770 | Common:2; Rare:105 | ||||
| chr4:168165127-168165308 | Common:1; Rare:47 | ||||
| chr4:168480406-168480522 | Common:1; Rare:23 | ||||
| chr4:169010125-169010474 | Common:4; Rare:112 | ||||
| chr4:169620373-169620609 | Common:2; Rare:92 | ||||
| chr4:169620842-169620954 | Rare:22 | ||||
| chr4:170026287-170026618 | Common:4; Rare:128 | ||||
| chr4:173370690-173370982 | Common:2; Rare:74 |