| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179820713-179821117 | Common:6; Rare:148; Clinvar:7; Clinvar (benign):2 | ||||
| chr5:179821124-179821138 | Rare:4 | ||||
| chr5:179858792-179859047 | Rare:136 | ||||
| chr5:180071671-180071835 | Common:1; Rare:71 | ||||
| chr5:180494205-180494379 | Common:2; Rare:50 | ||||
| chr5:180802780-180802997 | Common:8; Rare:82 | ||||
| chr5:180810081-180810254 | Common:4; Rare:51 | ||||
| chr5:180861146-180861405 | Common:2; Rare:103 | ||||
| chr5:181040084-181040307 | Rare:42 | ||||
| chr5:181223122-181223313 | Rare:65 | ||||
| chr5:181223631-181223749 | Common:3; Rare:28 | ||||
| chr5:181243685-181243950 | Common:4; Rare:96 | ||||
| chr5:181261041-181261262 | Rare:74 | ||||
| chr6:292000-292320 | Common:1; Rare:53 | ||||
| chr6:292414-292558 | Rare:46 |