| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196062587-196062921 | Common:2; Rare:84 | ||||
| chr3:196082024-196082222 | Common:1; Rare:85 | ||||
| chr3:196287606-196287851 | Common:1; Rare:81 | ||||
| chr3:196318028-196318372 | Common:1; Rare:139; Clinvar (pathogenic):1 | ||||
| chr3:196338360-196338699 | Rare:80 | ||||
| chr3:196432398-196432590 | Common:1; Rare:82 | ||||
| chr3:196503648-196503952 | Common:5; Rare:106 | ||||
| chr3:196568518-196568676 | Common:3; Rare:41 | ||||
| chr3:196712188-196712411 | Common:4; Rare:78 | ||||
| chr3:196867748-196867954 | Rare:72 | ||||
| chr3:196941860-196942175 | Common:3; Rare:90 | ||||
| chr3:196942355-196942713 | Common:1; Rare:159 | ||||
| chr3:197029783-197029961 | Common:1; Rare:59 | ||||
| chr3:197298100-197298289 | Common:1; Rare:69 | ||||
| chr3:197555954-197556107 | Rare:38 |