| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139404056-139404182 | Rare:46 | ||||
| chr5:139482598-139482943 | Rare:47 | ||||
| chr5:139561733-139561813 | Rare:30 | ||||
| chr5:140107514-140107856 | Rare:118 | ||||
| chr5:140564296-140564462 | Common:1; Rare:48 | ||||
| chr5:140633158-140633548 | Common:1; Rare:59 | ||||
| chr5:140647585-140647924 | Common:5; Rare:139; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664750-140664943 | Common:2; Rare:56 | ||||
| chr5:140691309-140691657 | Common:1; Rare:125; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141172537-141172671 | Common:1; Rare:27 | ||||
| chr5:141245221-141245406 | Rare:43 | ||||
| chr5:141320754-141320910 | Common:1; Rare:50 | ||||
| chr5:141475641-141476029 | Common:2; Rare:69 | ||||
| chr5:141618910-141619270 | Common:1; Rare:116; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:141636803-141637011 | Common:2; Rare:93 |