| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42879577-42879940 | Rare:106 | ||||
| chr6:42890802-42890933 | Rare:47 | ||||
| chr6:42929112-42929175 | Rare:17 | ||||
| chr6:42929209-42929601 | Common:4; Rare:117 | ||||
| chr6:42984284-42984635 | Rare:91 | ||||
| chr6:43013869-43014287 | Common:2; Rare:92 | ||||
| chr6:43053796-43054035 | Common:1; Rare:70; Clinvar:5 | ||||
| chr6:43427481-43427572 | Rare:27 | ||||
| chr6:43427799-43427922 | Rare:37 | ||||
| chr6:43516858-43517138 | Common:4; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576190 | Rare:95; Clinvar:4 | ||||
| chr6:43629165-43629484 | Common:2; Rare:92 | ||||
| chr6:43687757-43687912 | Common:2; Rare:59 | ||||
| chr6:43770061-43770229 | Common:3; Rare:51 | ||||
| chr6:43771906-43771990 | Rare:18 |