| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:31532085-31532345 | Common:2; Rare:74 | ||||
| chr5:34656164-34656454 | Common:3; Rare:73 | ||||
| chr5:34915463-34915776 | Common:1; Rare:91 | ||||
| chr5:36151881-36152172 | Rare:90 | ||||
| chr5:38845767-38846078 | Common:1; Rare:79 | ||||
| chr5:43603093-43603203 | Rare:25 | ||||
| chr5:50667760-50667894 | Common:1; Rare:43 | ||||
| chr5:53109748-53109871 | Common:1; Rare:59; Clinvar:1 | ||||
| chr5:55307644-55308010 | Common:4; Rare:120 | ||||
| chr5:60945019-60945238 | Common:5; Rare:88; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162395-61162490 | Common:1; Rare:22 | ||||
| chr5:62403879-62404029 | Common:3; Rare:46 | ||||
| chr5:64768611-64768955 | Common:4; Rare:89 | ||||
| chr5:65563123-65563316 | Common:3; Rare:70 | ||||
| chr5:65722043-65722197 | Common:2; Rare:52 |