| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127047437-127047626 | Common:4; Rare:44 | ||||
| chr3:127075690-127075849 | Rare:41 | ||||
| chr3:128489103-128489256 | Rare:33 | ||||
| chr3:128845807-128845994 | Common:2; Rare:36 | ||||
| chr3:130111459-130111674 | Common:3; Rare:59 | ||||
| chr3:131361588-131361912 | Common:3; Rare:97 | ||||
| chr3:131981253-131981379 | Common:2; Rare:18 | ||||
| chr3:132320955-132321128 | Common:2; Rare:27 | ||||
| chr3:132345787-132345908 | Common:2; Rare:15 | ||||
| chr3:141455850-141456140 | Common:1; Rare:38 | ||||
| chr3:144757689-144757826 | Common:3; Rare:38 | ||||
| chr3:153281721-153281979 | Common:4; Rare:64 | ||||
| chr3:157174928-157175223 | Common:3; Rare:129 | ||||
| chr3:169764853-169764869 | Rare:10; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr3:169764972-169765181 | Common:1; Rare:87; Clinvar:7; Clinvar (pathogenic):4 |