| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915445-34915766 | Common:1; Rare:88 | ||||
| chr5:34929668-34929915 | Rare:82 | ||||
| chr5:35856803-35856931 | Rare:19 | ||||
| chr5:36151770-36152201 | Rare:113 | ||||
| chr5:36242140-36242378 | Common:1; Rare:61 | ||||
| chr5:36606468-36606680 | Rare:36 | ||||
| chr5:36876644-36877172 | Common:1; Rare:159; Clinvar:3; Clinvar (benign):4 | ||||
| chr5:37371040-37371379 | Common:2; Rare:83 | ||||
| chr5:37379187-37379364 | Rare:46 | ||||
| chr5:38557225-38557358 | Rare:35 | ||||
| chr5:38845706-38846053 | Common:2; Rare:90 | ||||
| chr5:39074363-39074510 | Common:1; Rare:63 | ||||
| chr5:39274453-39274471 | Rare:3 | ||||
| chr5:39425010-39425322 | Common:2; Rare:67 | ||||
| chr5:40679303-40679445 | Common:1; Rare:28 |