| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186144257-186144496 | Common:2; Rare:50 | ||||
| chr4:186144625-186144672 | Rare:11 | ||||
| chr4:186145119-186145244 | Common:1; Rare:28 | ||||
| chr4:186190882-186191074 | Common:3; Rare:39 | ||||
| chr4:186191153-186191745 | Common:10; Rare:161; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186191767-186191937 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:189940453-189940526 | Common:1; Rare:9 | ||||
| chr4:189940532-189941134 | Common:19; Rare:211 | ||||
| chr4:189941167-189941199 | Rare:4 | ||||
| chr5:218081-218377 | Common:4; Rare:125; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:271242-271271 | Rare:6 | ||||
| chr5:271276-271763 | Common:5; Rare:190 | ||||
| chr5:321505-321796 | Common:4; Rare:66 | ||||
| chr5:322073-322294 | Rare:48 | ||||
| chr5:322340-322676 | Rare:76 |