| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:38556371-38556809 | Common:3; Rare:148 | ||||
| chr5:38557220-38557280 | Rare:12 | ||||
| chr5:38557462-38557501 | Rare:7 | ||||
| chr5:38845712-38846073 | Common:2; Rare:95 | ||||
| chr5:39073864-39074125 | Common:5; Rare:72 | ||||
| chr5:39074313-39074580 | Common:1; Rare:126 | ||||
| chr5:40679303-40679409 | Common:1; Rare:22 | ||||
| chr5:40679678-40679968 | Common:2; Rare:69 | ||||
| chr5:40755882-40756040 | Rare:43 | ||||
| chr5:40798152-40798448 | Common:1; Rare:116 | ||||
| chr5:40835173-40835398 | Common:2; Rare:89 | ||||
| chr5:41510456-41510807 | Common:1; Rare:98 | ||||
| chr5:41870354-41870632 | Common:2; Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:41870760-41870928 | Rare:42 | ||||
| chr5:41904003-41904391 | Common:2; Rare:124 |