| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197949893-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959986-197960244 | Common:1; Rare:91 | ||||
| chr4:337553-337833 | Common:1; Rare:65 | ||||
| chr4:499136-499344 | Common:3; Rare:84 | ||||
| chr4:674213-674552 | Common:2; Rare:156 | ||||
| chr4:932250-932487 | Common:2; Rare:93 | ||||
| chr4:1113543-1113632 | Common:1; Rare:33 | ||||
| chr4:1804518-1804969 | Common:3; Rare:154; Clinvar:2; Clinvar (benign):6 | ||||
| chr4:2468947-2469173 | Common:2; Rare:76 | ||||
| chr4:2798847-2799175 | Common:4; Rare:62 | ||||
| chr4:2934779-2934910 | Common:1; Rare:63 | ||||
| chr4:2963327-2963607 | Common:2; Rare:98 | ||||
| chr4:3074480-3074730 | Common:5; Rare:83 | ||||
| chr4:3385439-3385532 | Common:2; Rare:16 | ||||
| chr4:3385987-3386371 | Common:4; Rare:64 |