| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43067346-43067509 | Rare:22 | ||||
| chr5:43313376-43313665 | Common:3; Rare:76 | ||||
| chr5:43483837-43483947 | Common:1; Rare:41 | ||||
| chr5:43515021-43515289 | Common:4; Rare:90 | ||||
| chr5:43603076-43603266 | Rare:46 | ||||
| chr5:44388354-44388380 | Rare:6 | ||||
| chr5:44808655-44809043 | Common:2; Rare:136 | ||||
| chr5:50665804-50665933 | Rare:17 | ||||
| chr5:50667477-50667570 | Rare:31 | ||||
| chr5:50667768-50667918 | Common:1; Rare:47 | ||||
| chr5:52787832-52787988 | Common:1; Rare:30 | ||||
| chr5:52989224-52989408 | Common:4; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109725-53109909 | Common:1; Rare:92; Clinvar:2 | ||||
| chr5:53560614-53560728 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:54310496-54310711 | Rare:67 |