| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33289186-33289653 | Common:4; Rare:101 | ||||
| chr6:33298930-33299052 | Rare:31 | ||||
| chr6:33322934-33323265 | Common:5; Rare:96 | ||||
| chr6:33417879-33417948 | Rare:29 | ||||
| chr6:33418037-33418464 | Common:2; Rare:103 | ||||
| chr6:33454406-33454593 | Rare:54 | ||||
| chr6:33711631-33711770 | Common:1; Rare:53; Clinvar (benign):1 | ||||
| chr6:34426017-34426145 | Common:4; Rare:62; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696716-34696988 | Common:1; Rare:64 | ||||
| chr6:34757257-34757545 | Common:2; Rare:72 | ||||
| chr6:34887966-34888091 | Common:1; Rare:36 | ||||
| chr6:36442915-36443087 | Common:2; Rare:70 | ||||
| chr6:36594124-36594378 | Common:4; Rare:97 | ||||
| chr6:36678415-36678746 | Common:1; Rare:74 | ||||
| chr6:36874790-36875168 | Common:1; Rare:80 |