| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115841505-115841603 | Common:2; Rare:65 | ||||
| chr5:115841836-115842105 | Common:4; Rare:85 | ||||
| chr5:116085359-116085467 | Rare:27 | ||||
| chr5:119070872-119071207 | Common:3; Rare:106 | ||||
| chr5:119071324-119071504 | Rare:72 | ||||
| chr5:119268611-119268840 | Common:1; Rare:60 | ||||
| chr5:119355767-119356026 | Common:3; Rare:72 | ||||
| chr5:119452421-119452785 | Common:1; Rare:170; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr5:122845508-122845678 | Common:3; Rare:66 | ||||
| chr5:123036533-123036765 | Common:1; Rare:70 | ||||
| chr5:123511978-123512278 | Common:1; Rare:83 | ||||
| chr5:124748809-124748997 | Common:1; Rare:49 | ||||
| chr5:126594217-126594370 | Rare:37 | ||||
| chr5:126595139-126595361 | Common:5; Rare:100; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr5:126776917-126777223 | Common:2; Rare:115; Clinvar:4; Clinvar (benign):4 |