| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:168318661-168318828 | Rare:38 | ||||
| chr4:168318832-168318849 | Rare:2 | ||||
| chr4:168480384-168480639 | Common:1; Rare:41 | ||||
| chr4:168831985-168832106 | Common:2; Rare:33 | ||||
| chr4:168894413-168894662 | Rare:55; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:168898281-168898549 | Common:1; Rare:67; Clinvar:3 | ||||
| chr4:168921359-168921741 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:169010233-169010434 | Common:1; Rare:59 | ||||
| chr4:169270864-169271169 | Common:2; Rare:95 | ||||
| chr4:169612570-169612783 | Common:4; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620391-169620730 | Common:2; Rare:116 | ||||
| chr4:173168064-173168531 | Common:5; Rare:86 | ||||
| chr4:173169077-173169321 | Common:2; Rare:80 | ||||
| chr4:173333622-173333878 | Common:1; Rare:70 | ||||
| chr4:173369792-173369935 | Common:1; Rare:48 |