| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36876642-36876988 | Common:1; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:37371048-37371379 | Common:2; Rare:80 | ||||
| chr5:37379059-37379364 | Common:3; Rare:72 | ||||
| chr5:38557236-38557334 | Rare:24 | ||||
| chr5:38845769-38846049 | Common:1; Rare:72 | ||||
| chr5:39074329-39074510 | Common:1; Rare:85 | ||||
| chr5:39424856-39425044 | Common:1; Rare:52 | ||||
| chr5:39425116-39425308 | Common:2; Rare:48 | ||||
| chr5:40755889-40756056 | Rare:45 | ||||
| chr5:40798152-40798435 | Common:1; Rare:110 | ||||
| chr5:40835184-40835406 | Common:2; Rare:89 | ||||
| chr5:41510762-41510802 | Common:1; Rare:5 | ||||
| chr5:41870360-41870707 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:41903965-41904368 | Common:1; Rare:118 | ||||
| chr5:41925181-41925327 | Common:1; Rare:58 |