| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158801984-158802111 | Common:2; Rare:63 | ||||
| chr3:160399196-160399310 | Rare:31; Clinvar:1 | ||||
| chr3:160399500-160399687 | Rare:48; Clinvar:1 | ||||
| chr3:160449737-160450075 | Common:2; Rare:114 | ||||
| chr3:160565517-160565789 | Common:2; Rare:103 | ||||
| chr3:161221184-161221326 | Rare:45 | ||||
| chr3:167734849-167735226 | Common:3; Rare:119 | ||||
| chr3:167735611-167735740 | Rare:30 | ||||
| chr3:169773348-169773443 | Rare:32 | ||||
| chr3:169966628-169966858 | Common:2; Rare:90 | ||||
| chr3:170181721-170181847 | Rare:43 | ||||
| chr3:170222358-170222572 | Common:1; Rare:75 | ||||
| chr3:170870163-170870267 | Rare:58 | ||||
| chr3:172750512-172750806 | Common:3; Rare:82 | ||||
| chr3:179347605-179347753 | Common:1; Rare:34 |