| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52770867-52771152 | Common:12; Rare:248 | ||||
| chr3:52897475-52897802 | Rare:194 | ||||
| chr3:53045210-53045750 | Common:9; Rare:368 | ||||
| chr3:53045859-53046190 | Common:7; Rare:206 | ||||
| chr3:53046575-53046679 | Common:1; Rare:20 | ||||
| chr3:53046768-53047168 | Common:5; Rare:102 | ||||
| chr3:53130333-53130584 | Common:3; Rare:239; Clinvar:4; Clinvar (benign):9 | ||||
| chr3:53155700-53156086 | Rare:186 | ||||
| chr3:53160435-53160782 | Common:2; Rare:127 | ||||
| chr3:53161009-53161383 | Common:13; Rare:213 | ||||
| chr3:53161396-53161803 | Rare:128 | ||||
| chr3:53255844-53256214 | Common:10; Rare:324 | ||||
| chr3:53347455-53347905 | Common:9; Rare:371 | ||||
| chr3:53494031-53494442 | Common:12; Rare:231 | ||||
| chr3:53494390-53495040 | Common:5; Rare:365 |