| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:56557081-56557238 | Common:2; Rare:61 | ||||
| chr3:56682787-56683012 | Common:2; Rare:82 | ||||
| chr3:56683014-56683065 | Rare:23 | ||||
| chr3:56683226-56683370 | Common:2; Rare:53 | ||||
| chr3:57227600-57227911 | Common:3; Rare:105 | ||||
| chr3:57259701-57259871 | Common:1; Rare:36 | ||||
| chr3:57556000-57556321 | Rare:80 | ||||
| chr3:57597326-57597744 | Common:4; Rare:125 | ||||
| chr3:57692966-57693160 | Common:1; Rare:56 | ||||
| chr3:57756045-57756324 | Rare:73 | ||||
| chr3:58210811-58211234 | Common:4; Rare:102 | ||||
| chr3:58237410-58237576 | Common:7; Rare:52 | ||||
| chr3:58433794-58434019 | Common:1; Rare:84; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58577421-58577734 | Common:2; Rare:48 | ||||
| chr3:61251364-61251594 | Common:4; Rare:55 |