| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139561100-139561409 | Common:1; Rare:123 | ||||
| chr5:139561723-139561794 | Rare:34 | ||||
| chr5:140303048-140303171 | Common:1; Rare:40 | ||||
| chr5:140557404-140557510 | Rare:64 | ||||
| chr5:140564573-140564863 | Rare:78 | ||||
| chr5:140647585-140647889 | Common:5; Rare:124; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664717-140664907 | Common:3; Rare:48 | ||||
| chr5:140691309-140691651 | Common:1; Rare:121; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:141320742-141320959 | Common:2; Rare:75 | ||||
| chr5:141636810-141636997 | Common:2; Rare:82 | ||||
| chr5:141680827-141681145 | Common:1; Rare:66 | ||||
| chr5:141682187-141682297 | Common:1; Rare:33 | ||||
| chr5:141923570-141923927 | Common:1; Rare:104 | ||||
| chr5:142324997-142325293 | Rare:92 | ||||
| chr5:142326040-142326140 | Common:1; Rare:21 |