| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34008080-34008228 | Common:2; Rare:51; Clinvar:1 | ||||
| chr5:34915208-34915352 | Rare:39 | ||||
| chr5:34915464-34915753 | Common:1; Rare:75 | ||||
| chr5:36066797-36067067 | Common:1; Rare:69 | ||||
| chr5:36151827-36152270 | Rare:130 | ||||
| chr5:36606543-36606660 | Rare:21 | ||||
| chr5:36876650-36876885 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37249344-37249659 | Common:1; Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371001-37371387 | Common:2; Rare:102 | ||||
| chr5:37379184-37379364 | Rare:47 | ||||
| chr5:39074373-39074480 | Common:1; Rare:43 | ||||
| chr5:40798152-40798435 | Common:1; Rare:110 | ||||
| chr5:40835173-40835320 | Common:2; Rare:60 | ||||
| chr5:40835322-40835341 | Rare:5 | ||||
| chr5:41870377-41870553 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 |