| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115841803-115842020 | Common:3; Rare:72 | ||||
| chr5:118988512-118988713 | Common:1; Rare:73 | ||||
| chr5:119268604-119268829 | Common:1; Rare:62 | ||||
| chr5:122077965-122078145 | Rare:40 | ||||
| chr5:122078253-122078497 | Common:1; Rare:53 | ||||
| chr5:123423309-123423618 | Rare:111 | ||||
| chr5:127030511-127030764 | Common:2; Rare:61 | ||||
| chr5:131165095-131165382 | Common:3; Rare:106; Clinvar (benign):2 | ||||
| chr5:131263625-131263750 | Rare:30 | ||||
| chr5:131263900-131264148 | Common:1; Rare:96 | ||||
| chr5:131635188-131635430 | Common:1; Rare:92 | ||||
| chr5:131796936-131797206 | Rare:79 | ||||
| chr5:132294244-132294413 | Common:1; Rare:40 | ||||
| chr5:132369897-132369942 | Rare:16; Clinvar:1 | ||||
| chr5:132410815-132411036 | Common:1; Rare:49 |