| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156291707-156292118 | Common:4; Rare:120 | ||||
| chr3:156674352-156674659 | Common:3; Rare:94 | ||||
| chr3:156826028-156826295 | Common:3; Rare:68 | ||||
| chr3:157159451-157159510 | Common:1; Rare:22 | ||||
| chr3:157160127-157160244 | Rare:44 | ||||
| chr3:157436789-157436922 | Common:1; Rare:31 | ||||
| chr3:157436928-157436983 | Common:1; Rare:16 | ||||
| chr3:158105706-158105931 | Common:5; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:158106039-158106074 | Rare:17 | ||||
| chr3:158110018-158110149 | Rare:27 | ||||
| chr3:158802011-158802294 | Common:3; Rare:114 | ||||
| chr3:159764300-159764420 | Common:1; Rare:31 | ||||
| chr3:160399153-160399324 | Rare:47; Clinvar:2 | ||||
| chr3:160399476-160399715 | Rare:70; Clinvar:2 | ||||
| chr3:160449517-160449624 | Rare:20 |