| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43628586-43629101 | Common:2; Rare:241 | ||||
| chr6:43629193-43629555 | Common:1; Rare:100 | ||||
| chr6:43630017-43630222 | Common:1; Rare:45 | ||||
| chr6:43635728-43635881 | Common:2; Rare:35 | ||||
| chr6:43644870-43645470 | Common:3; Rare:187; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr6:43687731-43687871 | Common:1; Rare:60 | ||||
| chr6:43770504-43770782 | Common:1; Rare:59; Clinvar:1 | ||||
| chr6:43771115-43772105 | Common:9; Rare:343 | ||||
| chr6:44126710-44127020 | Common:1; Rare:79 | ||||
| chr6:44127339-44127663 | Common:4; Rare:93 | ||||
| chr6:44219475-44219670 | Common:2; Rare:54 | ||||
| chr6:44223340-44223650 | Common:1; Rare:83 | ||||
| chr6:44246854-44247141 | Common:5; Rare:122 | ||||
| chr6:44247343-44248046 | Common:10; Rare:419 | ||||
| chr6:44256890-44257210 | Common:3; Rare:73 |