| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127030509-127030764 | Common:2; Rare:61 | ||||
| chr5:127073465-127073522 | Common:1; Rare:14 | ||||
| chr5:127517521-127517745 | Common:4; Rare:95 | ||||
| chr5:128965451-128965590 | Common:2; Rare:39 | ||||
| chr5:131170692-131171002 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr5:131252965-131253065 | Common:1; Rare:21 | ||||
| chr5:131635069-131635430 | Common:1; Rare:127 | ||||
| chr5:131796962-131797221 | Rare:71 | ||||
| chr5:132369595-132369767 | Common:4; Rare:50; Clinvar (benign):1 | ||||
| chr5:132410603-132410995 | Common:1; Rare:81 | ||||
| chr5:132490754-132491020 | Rare:68 | ||||
| chr5:132830617-132830717 | Rare:24 | ||||
| chr5:132866471-132866705 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963489-132963755 | Rare:72 | ||||
| chr5:132963826-132963992 | Common:1; Rare:57 |