| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33314155-33314312 | Common:5; Rare:55 | ||||
| chr6:33317730-33317907 | Rare:58 | ||||
| chr6:33322890-33323246 | Common:10; Rare:228 | ||||
| chr6:33391180-33391540 | Common:3; Rare:105 | ||||
| chr6:33391693-33391984 | Common:3; Rare:77 | ||||
| chr6:33410070-33410770 | Common:4; Rare:302 | ||||
| chr6:33410869-33411083 | Rare:74 | ||||
| chr6:33417864-33418463 | Common:4; Rare:295 | ||||
| chr6:33454366-33454638 | Common:1; Rare:141 | ||||
| chr6:33620040-33620512 | Common:7; Rare:128 | ||||
| chr6:33711600-33711776 | Common:1; Rare:62; Clinvar (benign):2 | ||||
| chr6:33788180-33788610 | Common:3; Rare:202 | ||||
| chr6:33789059-33789183 | Rare:70; Clinvar (pathogenic):1 | ||||
| chr6:34236706-34237246 | Common:6; Rare:305 | ||||
| chr6:34237263-34237657 | Common:4; Rare:215 |