| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:122845503-122845625 | Common:3; Rare:48 | ||||
| chr5:123423342-123423582 | Rare:72 | ||||
| chr5:124748753-124749051 | Common:3; Rare:65 | ||||
| chr5:126595192-126595368 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):9 | ||||
| chr5:126776917-126777181 | Common:1; Rare:102; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:127517504-127517693 | Common:6; Rare:87 | ||||
| chr5:128538178-128538387 | Common:5; Rare:68 | ||||
| chr5:129094471-129094759 | Common:3; Rare:115 | ||||
| chr5:131165204-131165382 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr5:131170678-131171013 | Common:1; Rare:75; Clinvar (benign):2 | ||||
| chr5:131635215-131635485 | Common:1; Rare:96 | ||||
| chr5:131796990-131797192 | Rare:53 | ||||
| chr5:132257476-132257708 | Common:7; Rare:56 | ||||
| chr5:132866364-132866673 | Common:1; Rare:96 | ||||
| chr5:133051851-133052189 | Rare:118 |