| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124748753-124749004 | Common:2; Rare:55 | ||||
| chr5:126423322-126423613 | Rare:82 | ||||
| chr5:126595183-126595355 | Common:4; Rare:79; Clinvar:4; Clinvar (benign):9 | ||||
| chr5:127290705-127290852 | Rare:31 | ||||
| chr5:131170708-131171002 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr5:131263894-131264111 | Common:1; Rare:79 | ||||
| chr5:131635149-131635439 | Common:1; Rare:110 | ||||
| chr5:131796943-131797231 | Rare:81 | ||||
| chr5:132257475-132257737 | Common:8; Rare:69 | ||||
| chr5:132369589-132369759 | Common:3; Rare:52 | ||||
| chr5:132410601-132410991 | Common:1; Rare:78 | ||||
| chr5:132490771-132491020 | Rare:64 | ||||
| chr5:132556804-132557026 | Common:1; Rare:77; Clinvar:1 | ||||
| chr5:132737492-132737608 | Rare:39 | ||||
| chr5:132866470-132866686 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 |