| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185425864-185426313 | Common:4; Rare:146 | ||||
| chr4:185471070-185471417 | Common:10; Rare:42 | ||||
| chr4:185535414-185535632 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:185775228-185775507 | Common:2; Rare:42 | ||||
| chr4:185775667-185775955 | Common:1; Rare:38 | ||||
| chr4:185811665-185812003 | Common:1; Rare:66 | ||||
| chr4:185812005-185812037 | Common:1; Rare:5 | ||||
| chr4:186191472-186191814 | Common:6; Rare:113; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723754-186723953 | Common:5; Rare:80 | ||||
| chr4:189940649-189941004 | Common:14; Rare:131 | ||||
| chr5:218083-218414 | Common:4; Rare:132; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:443084-443272 | Common:10; Rare:85 | ||||
| chr5:612178-612358 | Rare:73 | ||||
| chr5:693295-693586 | Common:6; Rare:87 | ||||
| chr5:892529-892947 | Common:5; Rare:126 |