| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:112205846-112206378 | Common:20; Rare:278 | ||||
| chr5:112707167-112707698 | Common:42; Rare:723; Clinvar:348; Clinvar (benign):76; Clinvar (pathogenic):5 | ||||
| chr5:112707923-112708369 | Common:1; Rare:156; Clinvar (benign):2 | ||||
| chr5:112737107-112737754 | Common:4; Rare:158; Clinvar (benign):6 | ||||
| chr5:112737756-112737930 | Rare:159; Clinvar:6; Clinvar (benign):11 | ||||
| chr5:112737944-112738681 | Common:4; Rare:405; Clinvar:9; Clinvar (benign):10 | ||||
| chr5:112861030-112861568 | Common:31; Rare:742 | ||||
| chr5:112920810-112921250 | Common:1; Rare:116 | ||||
| chr5:112921197-112921754 | Common:19; Rare:629 | ||||
| chr5:112921783-112922140 | Common:2; Rare:133 | ||||
| chr5:112922151-112922603 | Common:6; Rare:365 | ||||
| chr5:112975819-112976310 | Common:4; Rare:153 | ||||
| chr5:112976400-112977244 | Common:24; Rare:1506 | ||||
| chr5:112977415-112978380 | Common:9; Rare:283 | ||||
| chr5:113513380-113513802 | Common:3; Rare:216 |