| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:109689859-109690071 | Common:1; Rare:75 | ||||
| chr5:110738925-110739107 | Common:4; Rare:137 | ||||
| chr5:110739340-110739720 | Common:7; Rare:181; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:111092203-111092416 | Common:2; Rare:111; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:111511720-111512334 | Common:4; Rare:152 | ||||
| chr5:111512388-111512793 | Common:6; Rare:257 | ||||
| chr5:111757168-111757335 | Common:10; Rare:47 | ||||
| chr5:111757627-111757872 | Common:2; Rare:163 | ||||
| chr5:112707276-112707665 | Common:17; Rare:300; Clinvar:149; Clinvar (benign):31; Clinvar (pathogenic):2 | ||||
| chr5:112861095-112861376 | Common:8; Rare:207 | ||||
| chr5:112921532-112921694 | Common:8; Rare:91 | ||||
| chr5:112976442-112976881 | Common:6; Rare:386 | ||||
| chr5:113513624-113513763 | Rare:86 | ||||
| chr5:115262818-115262919 | Common:1; Rare:50 | ||||
| chr5:115544643-115545014 | Common:4; Rare:275 |