| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:126423343-126423510 | Rare:42 | ||||
| chr5:126595173-126595380 | Common:4; Rare:89; Clinvar:5; Clinvar (benign):9 | ||||
| chr5:126600856-126600993 | Common:1; Rare:65 | ||||
| chr5:126776879-126777221 | Common:3; Rare:133; Clinvar:4; Clinvar (benign):6 | ||||
| chr5:127030539-127030681 | Common:1; Rare:35 | ||||
| chr5:127073465-127073584 | Common:3; Rare:42 | ||||
| chr5:127290698-127290893 | Rare:41 | ||||
| chr5:127517495-127517728 | Common:7; Rare:101 | ||||
| chr5:129094471-129094759 | Common:3; Rare:115 | ||||
| chr5:131165141-131165407 | Common:3; Rare:107; Clinvar (benign):2 | ||||
| chr5:131170670-131171008 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr5:131263798-131264117 | Common:2; Rare:118 | ||||
| chr5:131635109-131635735 | Common:1; Rare:202 | ||||
| chr5:131796932-131797221 | Rare:81 | ||||
| chr5:132294108-132294165 | Rare:11 |