| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:136196821-136197000 | Common:1; Rare:58 | ||||
| chr3:136250225-136250402 | Common:3; Rare:77; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:136250562-136250774 | Common:3; Rare:58; Clinvar (benign):1 | ||||
| chr3:136752340-136752763 | Common:1; Rare:142 | ||||
| chr3:136818986-136819149 | Common:4; Rare:90 | ||||
| chr3:136861903-136862301 | Common:1; Rare:122 | ||||
| chr3:138114970-138115240 | Rare:57 | ||||
| chr3:138115532-138115718 | Common:4; Rare:50 | ||||
| chr3:138174262-138174662 | Common:4; Rare:125 | ||||
| chr3:138174836-138174975 | Common:2; Rare:33 | ||||
| chr3:138187156-138187560 | Common:1; Rare:112 | ||||
| chr3:138329760-138330100 | Common:1; Rare:70 | ||||
| chr3:138348190-138348740 | Common:2; Rare:142 | ||||
| chr3:138594166-138594484 | Rare:99 | ||||
| chr3:138608522-138608799 | Rare:63 |