| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9987282-9987928 | Common:14; Rare:332 | ||||
| chr3:10010150-10011451 | Common:7; Rare:501 | ||||
| chr3:10025838-10026238 | Common:7; Rare:92 | ||||
| chr3:10026220-10026652 | Common:3; Rare:464 | ||||
| chr3:10026560-10026994 | Common:9; Rare:194 | ||||
| chr3:10115436-10116173 | Common:32; Rare:816 | ||||
| chr3:10141430-10141955 | Common:14; Rare:605; Clinvar:109; Clinvar (benign):106 | ||||
| chr3:10141880-10142406 | Common:2; Rare:282; Clinvar:74; Clinvar (benign):61; Clinvar (pathogenic):22 | ||||
| chr3:10142437-10143443 | Common:22; Rare:658 | ||||
| chr3:10164651-10165051 | Common:5; Rare:244 | ||||
| chr3:10248120-10248634 | Common:26; Rare:637 | ||||
| chr3:10248636-10249036 | Common:3; Rare:108 | ||||
| chr3:10249246-10249890 | Common:4; Rare:449 | ||||
| chr3:10292651-10293296 | Common:17; Rare:542 | ||||
| chr3:10320995-10321433 | Common:6; Rare:382 |