| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:16761440-16761729 | Common:2; Rare:89 | ||||
| chr6:16761735-16762004 | Common:2; Rare:61 | ||||
| chr6:17280788-17281034 | Common:2; Rare:72 | ||||
| chr6:17289648-17289993 | Rare:63 | ||||
| chr6:17393421-17393734 | Common:1; Rare:85 | ||||
| chr6:17600267-17600409 | Common:2; Rare:48 | ||||
| chr6:17706633-17706672 | Rare:11 | ||||
| chr6:17706752-17707113 | Common:1; Rare:98 | ||||
| chr6:17986827-17986945 | Rare:26 | ||||
| chr6:18122624-18122763 | Common:1; Rare:32; Clinvar (benign):2 | ||||
| chr6:18155031-18155543 | Common:11; Rare:133; Clinvar:2 | ||||
| chr6:18264383-18264865 | Common:1; Rare:184 | ||||
| chr6:20212397-20212723 | Common:1; Rare:88 | ||||
| chr6:20401539-20401927 | Common:3; Rare:102 | ||||
| chr6:20534396-20534583 | Common:1; Rare:60 |