| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41053050-41053404 | Common:4; Rare:64 | ||||
| chr6:41072301-41072514 | Rare:62 | ||||
| chr6:41072532-41072897 | Rare:101 | ||||
| chr6:41921104-41921229 | Rare:33 | ||||
| chr6:42050354-42050547 | Common:1; Rare:55 | ||||
| chr6:42746064-42746336 | Rare:79 | ||||
| chr6:42879581-42879943 | Rare:105 | ||||
| chr6:42890794-42890942 | Rare:57 | ||||
| chr6:42929209-42929562 | Common:4; Rare:100 | ||||
| chr6:42984327-42984635 | Rare:78 | ||||
| chr6:43013869-43014329 | Common:2; Rare:101 | ||||
| chr6:43059820-43059890 | Rare:23 | ||||
| chr6:43060230-43060517 | Common:1; Rare:81 | ||||
| chr6:43427454-43427572 | Rare:33 | ||||
| chr6:43516778-43517112 | Common:6; Rare:117; Clinvar:2; Clinvar (benign):1 |