| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:123511954-123512262 | Common:1; Rare:90 | ||||
| chr5:124748758-124749046 | Common:3; Rare:64 | ||||
| chr5:126595192-126595319 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):7 | ||||
| chr5:127030521-127030736 | Common:2; Rare:49 | ||||
| chr5:127073471-127073523 | Common:1; Rare:11 | ||||
| chr5:127290656-127290844 | Rare:41 | ||||
| chr5:127517511-127517731 | Common:4; Rare:93 | ||||
| chr5:129094551-129094759 | Common:2; Rare:83 | ||||
| chr5:131165206-131165373 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chr5:131170698-131171002 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr5:131635146-131635446 | Common:1; Rare:113 | ||||
| chr5:131796936-131797221 | Rare:81 | ||||
| chr5:132369652-132369740 | Common:2; Rare:25 | ||||
| chr5:132369883-132369927 | Common:2; Rare:14; Clinvar (benign):2 | ||||
| chr5:132556821-132557020 | Common:1; Rare:70; Clinvar:1 |