| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:12008532-12008849 | Common:1; Rare:73 | ||||
| chr6:12289985-12290090 | Rare:10 | ||||
| chr6:13328478-13328633 | Common:5; Rare:67 | ||||
| chr6:13615159-13615769 | Common:3; Rare:248 | ||||
| chr6:13711044-13711366 | Common:2; Rare:127 | ||||
| chr6:13924891-13925007 | Common:1; Rare:44 | ||||
| chr6:15245802-15246070 | Common:1; Rare:85 | ||||
| chr6:15246141-15246286 | Rare:35 | ||||
| chr6:16761399-16761724 | Common:2; Rare:97 | ||||
| chr6:17393487-17393733 | Common:1; Rare:66 | ||||
| chr6:17600224-17600302 | Common:1; Rare:31 | ||||
| chr6:17706112-17706183 | Common:1; Rare:27 | ||||
| chr6:17706282-17706480 | Common:2; Rare:86 | ||||
| chr6:17706721-17706965 | Common:1; Rare:67 | ||||
| chr6:18122624-18122763 | Common:1; Rare:32; Clinvar (benign):2 |