| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:33134578-33134665 | Rare:14 | ||||
| chr2:33476338-33476691 | Common:5; Rare:74 | ||||
| chr2:33599217-33599445 | Common:1; Rare:87 | ||||
| chr2:36902680-36903046 | Rare:102 | ||||
| chr2:37084269-37084569 | Common:4; Rare:114 | ||||
| chr2:37231553-37231726 | Common:4; Rare:100; Clinvar (benign):4 | ||||
| chr2:37324698-37324950 | Common:1; Rare:100 | ||||
| chr2:37344582-37344741 | Common:1; Rare:63 | ||||
| chr2:38076132-38076228 | Rare:19 | ||||
| chr2:38751339-38751645 | Common:4; Rare:143 | ||||
| chr2:38875897-38876055 | Common:1; Rare:57 | ||||
| chr2:39437078-39437464 | Common:4; Rare:138 | ||||
| chr2:39665103-39665253 | Common:3; Rare:40 | ||||
| chr2:42169077-42169436 | Common:1; Rare:150 | ||||
| chr2:43595961-43596205 | Common:1; Rare:89 |