| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3126768-3127016 | Common:4; Rare:113; Clinvar (benign):4 | ||||
| chr3:4303301-4303637 | Common:3; Rare:134 | ||||
| chr3:4493169-4493533 | Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4978622-4978926 | Common:3; Rare:90 | ||||
| chr3:4979148-4979512 | Common:2; Rare:83 | ||||
| chr3:5187295-5187628 | Common:4; Rare:127 | ||||
| chr3:8501649-8501937 | Common:2; Rare:106 | ||||
| chr3:9362952-9363214 | Common:4; Rare:81 | ||||
| chr3:9363303-9363420 | Rare:22 | ||||
| chr3:9397427-9397685 | Rare:95 | ||||
| chr3:9397776-9397891 | Rare:24 | ||||
| chr3:9649251-9649565 | Common:1; Rare:113 | ||||
| chr3:9749839-9750018 | Common:1; Rare:62 | ||||
| chr3:9750204-9750291 | Common:1; Rare:28 | ||||
| chr3:9769894-9770041 | Common:1; Rare:40 |