| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177883973-177884170 | Common:1; Rare:13 | ||||
| chr5:177939455-177939514 | Rare:11 | ||||
| chr5:178209805-178210291 | Common:1; Rare:165 | ||||
| chr5:178228464-178228722 | Common:2; Rare:70 | ||||
| chr5:178605302-178605554 | Rare:40 | ||||
| chr5:179622360-179622486 | Common:1; Rare:42 | ||||
| chr5:179703379-179703635 | Common:1; Rare:45 | ||||
| chr5:179722772-179722829 | Common:1; Rare:19 | ||||
| chr5:179834044-179834398 | Common:10; Rare:108 | ||||
| chr5:180553445-180553552 | Common:1; Rare:24 | ||||
| chr5:180831551-180831748 | Common:2; Rare:81 | ||||
| chr6:1611901-1611946 | Common:1; Rare:20; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:1612191-1612545 | Common:2; Rare:79 | ||||
| chr6:1613424-1613743 | Common:2; Rare:61 | ||||
| chr6:2783418-2783673 | Common:2; Rare:91 |