| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9977044-9977209 | Common:1; Rare:33 | ||||
| chr3:10006588-10006664 | Rare:12 | ||||
| chr3:10017063-10017341 | Common:4; Rare:44 | ||||
| chr3:10017516-10017546 | Rare:9 | ||||
| chr3:10036118-10036319 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr3:10043256-10043509 | Common:2; Rare:70; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:10118734-10118782 | Rare:13 | ||||
| chr3:10282079-10282111 | Common:1; Rare:11 | ||||
| chr3:10301219-10301492 | Rare:83 | ||||
| chr3:10301906-10301930 | Rare:8 | ||||
| chr3:10303090-10303387 | Common:3; Rare:61 | ||||
| chr3:10308676-10308860 | Common:7; Rare:32 | ||||
| chr3:10308875-10308950 | Rare:8 | ||||
| chr3:10309901-10310186 | Common:3; Rare:53 | ||||
| chr3:10319522-10319831 | Common:3; Rare:54 |