| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42879583-42879943 | Rare:104 | ||||
| chr6:42890794-42890921 | Rare:47 | ||||
| chr6:42929131-42929202 | Rare:21 | ||||
| chr6:42929211-42929406 | Common:2; Rare:45 | ||||
| chr6:42929409-42929562 | Common:1; Rare:52 | ||||
| chr6:42984284-42984635 | Rare:91 | ||||
| chr6:43013822-43014285 | Common:2; Rare:116 | ||||
| chr6:43060252-43060555 | Common:1; Rare:83 | ||||
| chr6:43076122-43076479 | Rare:117 | ||||
| chr6:43182050-43182233 | Rare:52 | ||||
| chr6:43427436-43427576 | Rare:36 | ||||
| chr6:43516846-43517124 | Common:5; Rare:105; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575911-43576190 | Common:1; Rare:106; Clinvar:4 | ||||
| chr6:43687744-43687845 | Common:1; Rare:45 | ||||
| chr6:43770081-43770303 | Common:4; Rare:60 |