| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:195895879-195896055 | Common:2; Rare:122 | ||||
| chr3:195896050-195896520 | Common:4; Rare:139 | ||||
| chr3:195909510-195909970 | Common:12; Rare:278 | ||||
| chr3:196058601-196058891 | Rare:62 | ||||
| chr3:196081740-196081990 | Common:2; Rare:98 | ||||
| chr3:196081992-196082319 | Common:9; Rare:221 | ||||
| chr3:196287592-196288027 | Common:3; Rare:192 | ||||
| chr3:196317610-196318120 | Common:7; Rare:224; Clinvar (pathogenic):2 | ||||
| chr3:196318161-196318401 | Common:2; Rare:182 | ||||
| chr3:196338429-196338699 | Rare:72 | ||||
| chr3:196432273-196432635 | Common:2; Rare:215 | ||||
| chr3:196503477-196503956 | Common:13; Rare:248 | ||||
| chr3:196568484-196568906 | Common:10; Rare:255 | ||||
| chr3:196712216-196712437 | Common:8; Rare:147 | ||||
| chr3:196712500-196712850 | Common:6; Rare:171 |