| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51967374-51967615 | Common:1; Rare:55 | ||||
| chr3:51975046-51975126 | Common:1; Rare:29 | ||||
| chr3:51983230-51983517 | Common:1; Rare:65 | ||||
| chr3:51995732-51996022 | Common:3; Rare:91 | ||||
| chr3:52154376-52154524 | Common:1; Rare:39 | ||||
| chr3:52197972-52198165 | Rare:82 | ||||
| chr3:52239087-52239218 | Common:2; Rare:46 | ||||
| chr3:52287781-52287844 | Common:1; Rare:24 | ||||
| chr3:52536360-52536703 | Common:2; Rare:108 | ||||
| chr3:52685926-52686079 | Common:2; Rare:63 | ||||
| chr3:52705768-52706243 | Common:2; Rare:170 | ||||
| chr3:52770913-52771104 | Common:3; Rare:60 | ||||
| chr3:53130398-53130557 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347524-53347763 | Common:1; Rare:77 | ||||
| chr3:53891794-53892080 | Common:4; Rare:94 |