| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185811961-185811980 | Rare:2 | ||||
| chr4:185811984-185812172 | Common:1; Rare:31 | ||||
| chr4:185812175-185812276 | Rare:20 | ||||
| chr4:186191451-186191826 | Common:6; Rare:126; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723759-186723903 | Common:4; Rare:59 | ||||
| chr4:186726544-186726642 | Rare:21 | ||||
| chr4:189940588-189941012 | Common:16; Rare:145 | ||||
| chr5:218104-218415 | Common:4; Rare:124; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:443084-443269 | Common:10; Rare:84 | ||||
| chr5:612201-612358 | Rare:62 | ||||
| chr5:693289-693496 | Common:3; Rare:58 | ||||
| chr5:892529-892917 | Common:5; Rare:114 | ||||
| chr5:1345055-1345217 | Common:1; Rare:57 | ||||
| chr5:1445428-1445570 | Common:1; Rare:36 | ||||
| chr5:1799778-1799996 | Common:8; Rare:104 |