| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:1587776-1587899 | Rare:22 | ||||
| chr6:1588108-1588347 | Common:4; Rare:110 | ||||
| chr6:1611760-1612078 | Common:4; Rare:128; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr6:2623350-2623625 | Common:2; Rare:147 | ||||
| chr6:2630436-2630675 | Common:4; Rare:84 | ||||
| chr6:2630730-2631110 | Common:2; Rare:69 | ||||
| chr6:2631165-2631422 | Common:4; Rare:85 | ||||
| chr6:2634377-2634890 | Common:11; Rare:189 | ||||
| chr6:2857490-2858150 | Common:6; Rare:146 | ||||
| chr6:2876370-2876876 | Common:4; Rare:208 | ||||
| chr6:2940219-2940381 | Common:2; Rare:68 | ||||
| chr6:2982559-2982714 | Rare:26 | ||||
| chr6:2989334-2989626 | Common:2; Rare:46 | ||||
| chr6:2999143-2999369 | Common:2; Rare:75 | ||||
| chr6:3053622-3054022 | Common:6; Rare:265 |