| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40679698-40679975 | Common:1; Rare:63 | ||||
| chr5:40755884-40756018 | Rare:36 | ||||
| chr5:40798151-40798415 | Common:1; Rare:102 | ||||
| chr5:40835173-40835269 | Common:1; Rare:45 | ||||
| chr5:40841281-40841392 | Rare:27 | ||||
| chr5:40936317-40936670 | Common:2; Rare:96; Clinvar (pathogenic):2 | ||||
| chr5:41213462-41213713 | Rare:43 | ||||
| chr5:41870360-41870575 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:41904003-41904370 | Common:1; Rare:109 | ||||
| chr5:43043178-43043326 | Common:1; Rare:28 | ||||
| chr5:43064839-43065144 | Common:1; Rare:73 | ||||
| chr5:43067338-43067516 | Rare:24 | ||||
| chr5:43121410-43121667 | Common:1; Rare:99 | ||||
| chr5:43313393-43313670 | Common:3; Rare:74 | ||||
| chr5:43483837-43483913 | Common:1; Rare:31 |