| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157160660-157160970 | Common:10; Rare:126 | ||||
| chr3:157499390-157499920 | Common:5; Rare:174 | ||||
| chr3:158105737-158105922 | Common:5; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158110007-158110208 | Rare:75 | ||||
| chr3:158110250-158110480 | Common:4; Rare:114 | ||||
| chr3:158202870-158203490 | Common:1; Rare:236 | ||||
| chr3:158672557-158672877 | Common:8; Rare:136 | ||||
| chr3:158732117-158732268 | Common:6; Rare:81 | ||||
| chr3:158732406-158732708 | Common:4; Rare:151 | ||||
| chr3:158801976-158802171 | Common:4; Rare:165 | ||||
| chr3:159763170-159763420 | Rare:86 | ||||
| chr3:159763390-159763810 | Rare:178 | ||||
| chr3:159763883-159764216 | Common:6; Rare:204 | ||||
| chr3:160399144-160399362 | Rare:100; Clinvar:5 | ||||
| chr3:160399492-160400038 | Rare:222; Clinvar:1 |