| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:161221059-161221515 | Common:16; Rare:480 | ||||
| chr3:161221429-161221582 | Common:2; Rare:39 | ||||
| chr3:161221540-161222029 | Common:9; Rare:201 | ||||
| chr3:167734250-167734780 | Common:1; Rare:454; Clinvar (benign):2 | ||||
| chr3:167734794-167735262 | Common:25; Rare:818; Clinvar:5; Clinvar (benign):5 | ||||
| chr3:167735410-167735810 | Common:1; Rare:316; Clinvar:2 | ||||
| chr3:168094718-168095118 | Common:6; Rare:138 | ||||
| chr3:168095236-168096606 | Common:21; Rare:1149 | ||||
| chr3:169145980-169146280 | Common:3; Rare:52 | ||||
| chr3:169146300-169146450 | Rare:43 | ||||
| chr3:169146459-169146870 | Common:6; Rare:297 | ||||
| chr3:169147115-169147680 | Common:6; Rare:252 | ||||
| chr3:169662497-169663185 | Common:5; Rare:389 | ||||
| chr3:169772006-169772686 | Common:11; Rare:242 | ||||
| chr3:169772610-169772850 | Common:4; Rare:166 |