| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179806292-179806475 | Rare:63 | ||||
| chr5:179820761-179820922 | Common:3; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:180071712-180072057 | Common:1; Rare:126 | ||||
| chr5:180291918-180292242 | Common:2; Rare:129 | ||||
| chr5:180810083-180810301 | Common:5; Rare:65 | ||||
| chr5:181223116-181223319 | Rare:70 | ||||
| chr5:181223526-181223755 | Common:4; Rare:53 | ||||
| chr5:181243693-181243951 | Common:4; Rare:96 | ||||
| chr5:181261070-181261280 | Rare:73 | ||||
| chr6:291984-292081 | Common:1; Rare:15 | ||||
| chr6:693074-693198 | Rare:38 | ||||
| chr6:2245150-2245242 | Rare:16 | ||||
| chr6:2245585-2245834 | Rare:82 | ||||
| chr6:2765073-2765428 | Common:8; Rare:147 | ||||
| chr6:2765489-2765671 | Rare:94 |