| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115262837-115262889 | Rare:26 | ||||
| chr5:115816506-115816556 | Common:1; Rare:8 | ||||
| chr5:115816619-115816861 | Common:1; Rare:65 | ||||
| chr5:115841551-115841602 | Common:1; Rare:29 | ||||
| chr5:115841818-115842105 | Common:4; Rare:91 | ||||
| chr5:116084713-116085045 | Common:9; Rare:107 | ||||
| chr5:116085371-116085462 | Rare:21 | ||||
| chr5:119070880-119071207 | Common:3; Rare:104 | ||||
| chr5:119268604-119268821 | Common:1; Rare:61 | ||||
| chr5:120464149-120464398 | Common:1; Rare:76 | ||||
| chr5:122845508-122845621 | Common:3; Rare:44 | ||||
| chr5:123036621-123036865 | Common:2; Rare:63 | ||||
| chr5:123088932-123089295 | Common:11; Rare:153 | ||||
| chr5:123511943-123512271 | Common:1; Rare:101 | ||||
| chr5:126595179-126595366 | Common:4; Rare:85; Clinvar:5; Clinvar (benign):9 |