| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44246036-44246300 | Rare:71 | ||||
| chr6:44246902-44247195 | Common:4; Rare:124 | ||||
| chr6:44247850-44248071 | Common:5; Rare:65 | ||||
| chr6:44257471-44257633 | Rare:46 | ||||
| chr6:44387439-44387753 | Common:4; Rare:84 | ||||
| chr6:44387886-44388232 | Common:8; Rare:91 | ||||
| chr6:45377643-45377675 | Rare:13 | ||||
| chr6:45377805-45378183 | Common:2; Rare:124 | ||||
| chr6:46129772-46130166 | Common:5; Rare:126 | ||||
| chr6:46652712-46653022 | Rare:77 | ||||
| chr6:46735264-46735469 | Common:2; Rare:55 | ||||
| chr6:47477683-47478023 | Common:2; Rare:89; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:47478067-47478243 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:49463174-49463435 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284676-52285003 | Common:2; Rare:115 |