| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115841529-115841642 | Common:2; Rare:67 | ||||
| chr5:115841818-115842046 | Common:4; Rare:74 | ||||
| chr5:116084708-116085058 | Common:9; Rare:118 | ||||
| chr5:119070867-119071182 | Common:3; Rare:99 | ||||
| chr5:119268617-119268837 | Common:1; Rare:60 | ||||
| chr5:119355819-119356021 | Common:2; Rare:51 | ||||
| chr5:122845516-122845621 | Common:3; Rare:40 | ||||
| chr5:124748758-124748997 | Common:2; Rare:54 | ||||
| chr5:127030507-127030764 | Common:2; Rare:61 | ||||
| chr5:127290683-127290860 | Rare:38 | ||||
| chr5:131263918-131264109 | Rare:70 | ||||
| chr5:131635180-131635430 | Common:1; Rare:97 | ||||
| chr5:131796962-131797227 | Rare:73 | ||||
| chr5:132294111-132294411 | Common:1; Rare:73 | ||||
| chr5:132369575-132369966 | Common:8; Rare:130; Clinvar:6; Clinvar (benign):6 |