| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197949875-197950298 | Common:4; Rare:123; Clinvar (benign):2 | ||||
| chr3:197959989-197960245 | Common:1; Rare:90 | ||||
| chr4:499124-499333 | Common:3; Rare:84 | ||||
| chr4:673842-673964 | Rare:50 | ||||
| chr4:674212-674574 | Common:3; Rare:167 | ||||
| chr4:932259-932487 | Common:2; Rare:88 | ||||
| chr4:1289656-1289916 | Common:1; Rare:86 | ||||
| chr4:2468871-2469187 | Common:4; Rare:122 | ||||
| chr4:2843687-2843998 | Common:3; Rare:115 | ||||
| chr4:2934767-2934910 | Common:1; Rare:66 | ||||
| chr4:2963315-2963587 | Common:2; Rare:102 | ||||
| chr4:3074516-3074692 | Common:4; Rare:54 | ||||
| chr4:3385439-3385540 | Common:2; Rare:19 | ||||
| chr4:3386109-3386371 | Common:1; Rare:42 | ||||
| chr4:4248181-4248285 | Common:2; Rare:49 |