| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14651468-14651828 | Rare:109 | ||||
| chr3:14947372-14947563 | Common:3; Rare:92 | ||||
| chr3:15065060-15065358 | Common:2; Rare:112 | ||||
| chr3:15206057-15206278 | Rare:87 | ||||
| chr3:15427491-15427669 | Common:1; Rare:65 | ||||
| chr3:15601495-15601804 | Common:4; Rare:129; Clinvar:1 | ||||
| chr3:15859800-15860114 | Common:4; Rare:97 | ||||
| chr3:16264854-16265244 | Common:2; Rare:136 | ||||
| chr3:16884495-16884771 | Common:2; Rare:56 | ||||
| chr3:16884892-16885223 | Common:7; Rare:92 | ||||
| chr3:19946989-19947474 | Common:6; Rare:178 | ||||
| chr3:23916841-23917207 | Rare:138 | ||||
| chr3:25428107-25428391 | Rare:64 | ||||
| chr3:25783392-25783627 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr3:25789977-25790124 | Common:3; Rare:58 |