| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179678407-179678660 | Common:3; Rare:104 | ||||
| chr5:179698644-179699095 | Common:4; Rare:153 | ||||
| chr5:179806879-179807063 | Common:3; Rare:72 | ||||
| chr5:179820795-179820907 | Common:2; Rare:41; Clinvar (benign):1 | ||||
| chr5:179858788-179859040 | Rare:135 | ||||
| chr5:180353294-180353513 | Common:8; Rare:100 | ||||
| chr5:180802792-180802983 | Common:8; Rare:76 | ||||
| chr5:180810102-180810223 | Common:1; Rare:26 | ||||
| chr5:180861146-180861348 | Common:2; Rare:77 | ||||
| chr5:181223115-181223313 | Rare:68 | ||||
| chr5:181223633-181223761 | Common:3; Rare:29 | ||||
| chr5:181223876-181223990 | Rare:39 | ||||
| chr5:181243690-181243960 | Common:4; Rare:97 | ||||
| chr5:181261074-181261281 | Rare:72 | ||||
| chr6:292416-292536 | Rare:34 |