| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186726632-186726787 | Common:4; Rare:52 | ||||
| chr4:189940620-189940980 | Common:10; Rare:129 | ||||
| chr5:218114-218348 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:443063-443286 | Common:10; Rare:103 | ||||
| chr5:892720-892947 | Common:4; Rare:84 | ||||
| chr5:1799781-1799975 | Common:8; Rare:94 | ||||
| chr5:6632963-6633460 | Common:8; Rare:158; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868995-7869214 | Common:2; Rare:113; Clinvar (benign):1 | ||||
| chr5:9546043-9546376 | Common:7; Rare:75 | ||||
| chr5:10249863-10250188 | Common:16; Rare:149 | ||||
| chr5:10353600-10353910 | Common:3; Rare:112 | ||||
| chr5:31532032-31532352 | Common:3; Rare:90 | ||||
| chr5:32174248-32174379 | Common:1; Rare:51 | ||||
| chr5:33440632-33441093 | Common:7; Rare:127 | ||||
| chr5:34656133-34656478 | Common:3; Rare:88 |