| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:112707379-112707685 | Common:6; Rare:133; Clinvar:71; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr5:112861104-112861403 | Common:5; Rare:116 | ||||
| chr5:112921548-112921751 | Common:3; Rare:56 | ||||
| chr5:112922191-112922492 | Common:2; Rare:112 | ||||
| chr5:112976544-112976896 | Common:3; Rare:168 | ||||
| chr5:113203257-113203643 | Common:7; Rare:97 | ||||
| chr5:113294625-113294857 | Common:1; Rare:56 | ||||
| chr5:115262822-115262937 | Common:1; Rare:54 | ||||
| chr5:115544631-115545041 | Common:3; Rare:153 | ||||
| chr5:115816494-115816596 | Common:1; Rare:23 | ||||
| chr5:115816630-115816977 | Common:1; Rare:90 | ||||
| chr5:115841536-115842046 | Common:7; Rare:214 | ||||
| chr5:116084896-116085093 | Common:7; Rare:91 | ||||
| chr5:116085359-116085496 | Rare:40 | ||||
| chr5:116574810-116574918 | Common:2; Rare:37 |