| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36876650-36876889 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877002-36877155 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371053-37371198 | Rare:51 | ||||
| chr5:37379404-37379547 | Rare:44 | ||||
| chr5:38556472-38556882 | Common:3; Rare:142 | ||||
| chr5:38557204-38557386 | Rare:49 | ||||
| chr5:38845695-38846067 | Common:2; Rare:98 | ||||
| chr5:39074350-39074516 | Common:1; Rare:74 | ||||
| chr5:40679299-40679425 | Common:1; Rare:25 | ||||
| chr5:40679703-40679929 | Common:1; Rare:47 | ||||
| chr5:40755884-40756051 | Rare:44 | ||||
| chr5:40798152-40798326 | Rare:70 | ||||
| chr5:40835181-40835325 | Common:2; Rare:61 | ||||
| chr5:40841260-40841450 | Rare:58 | ||||
| chr5:41870362-41870639 | Common:2; Rare:88; Clinvar:2; Clinvar (benign):2 |