| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:35856654-35856931 | Rare:43 | ||||
| chr5:36151794-36152168 | Rare:97 | ||||
| chr5:36241622-36241961 | Common:4; Rare:118; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:36242162-36242325 | Common:1; Rare:41 | ||||
| chr5:36876630-36876952 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:37371031-37371197 | Rare:62 | ||||
| chr5:37379179-37379364 | Rare:47 | ||||
| chr5:37839710-37839974 | Rare:62 | ||||
| chr5:38556475-38556850 | Common:3; Rare:131 | ||||
| chr5:38557183-38557284 | Rare:24 | ||||
| chr5:38845704-38846073 | Common:2; Rare:97 | ||||
| chr5:39074339-39074522 | Common:1; Rare:88 | ||||
| chr5:39425010-39425308 | Common:2; Rare:65 | ||||
| chr5:40679292-40679450 | Common:1; Rare:32 | ||||
| chr5:40679703-40679952 | Common:1; Rare:55 |