| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37231559-37231726 | Common:4; Rare:95; Clinvar (benign):4 | ||||
| chr2:37324714-37324950 | Common:1; Rare:95 | ||||
| chr2:37671626-37671745 | Common:1; Rare:54 | ||||
| chr2:38076143-38076291 | Rare:38 | ||||
| chr2:38377243-38377519 | Common:2; Rare:108 | ||||
| chr2:38751307-38751592 | Common:5; Rare:139 | ||||
| chr2:38875886-38876059 | Common:1; Rare:63 | ||||
| chr2:39120992-39121141 | Rare:56 | ||||
| chr2:39437104-39437456 | Common:4; Rare:124 | ||||
| chr2:40512423-40512677 | Common:2; Rare:56 | ||||
| chr2:42169146-42169437 | Common:1; Rare:138 | ||||
| chr2:42792543-42792828 | Common:3; Rare:81 | ||||
| chr2:43595947-43596222 | Common:1; Rare:99 | ||||
| chr2:44361484-44362005 | Common:3; Rare:164 | ||||
| chr2:46617012-46617263 | Common:7; Rare:110 |