| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:116084943-116085067 | Common:3; Rare:60 | ||||
| chr5:116085403-116085461 | Rare:11 | ||||
| chr5:116574821-116574973 | Common:2; Rare:51 | ||||
| chr5:119070849-119071207 | Common:4; Rare:110 | ||||
| chr5:119268611-119268852 | Common:1; Rare:61 | ||||
| chr5:119355798-119356026 | Common:2; Rare:61 | ||||
| chr5:122845516-122845621 | Common:3; Rare:40 | ||||
| chr5:123036556-123036821 | Common:2; Rare:77 | ||||
| chr5:126423349-126423594 | Rare:70 | ||||
| chr5:126595178-126595337 | Common:3; Rare:77; Clinvar:5; Clinvar (benign):8 | ||||
| chr5:127030501-127030764 | Common:2; Rare:63 | ||||
| chr5:131170698-131171002 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr5:131263908-131264117 | Rare:76 | ||||
| chr5:131635159-131635439 | Common:1; Rare:106 | ||||
| chr5:131796917-131797215 | Rare:86 |