| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3799806-3799877 | Common:1; Rare:24 | ||||
| chr3:3799898-3800108 | Common:1; Rare:59 | ||||
| chr3:4303251-4303644 | Common:3; Rare:149 | ||||
| chr3:4467186-4467318 | Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:4493167-4493538 | Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:5122217-5122513 | Common:2; Rare:135 | ||||
| chr3:5187295-5187635 | Common:5; Rare:128 | ||||
| chr3:8501627-8501941 | Common:2; Rare:115 | ||||
| chr3:8677370-8677522 | Common:3; Rare:24 | ||||
| chr3:8682030-8682330 | Common:8; Rare:60 | ||||
| chr3:9013919-9014114 | Common:2; Rare:49 | ||||
| chr3:9216551-9216716 | Rare:30 | ||||
| chr3:9216726-9216864 | Common:3; Rare:49 | ||||
| chr3:9249540-9249750 | Common:1; Rare:43 | ||||
| chr3:9362923-9363168 | Common:2; Rare:76 |