| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:47477695-47478049 | Common:2; Rare:87; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:47478052-47478255 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:49463125-49463442 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:49550558-49550752 | Rare:42 | ||||
| chr6:50818594-50818932 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:52420133-52420356 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576992-52577324 | Common:6; Rare:120 | ||||
| chr6:52995255-52995820 | Common:4; Rare:229 | ||||
| chr6:53065332-53065487 | Common:1; Rare:57 | ||||
| chr6:53065548-53065745 | Rare:48 | ||||
| chr6:53348851-53349242 | Common:2; Rare:160 | ||||
| chr6:53545093-53545239 | Rare:43 | ||||
| chr6:53930140-53930203 | Rare:10 | ||||
| chr6:54846411-54846805 | Common:2; Rare:98 | ||||
| chr6:56542648-56542954 | Common:1; Rare:71 |