| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:37433148-37433249 | Common:2; Rare:34 | ||||
| chr6:41921104-41921264 | Rare:43 | ||||
| chr6:42217826-42217978 | Common:4; Rare:47 | ||||
| chr6:42879599-42879934 | Rare:97 | ||||
| chr6:42929240-42929549 | Common:3; Rare:82 | ||||
| chr6:43013869-43014276 | Common:2; Rare:89 | ||||
| chr6:43516883-43517119 | Common:4; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43576003-43576289 | Common:1; Rare:102; Clinvar:9 | ||||
| chr6:43635748-43635866 | Common:1; Rare:29 | ||||
| chr6:43687746-43688018 | Common:2; Rare:85 | ||||
| chr6:43770054-43770237 | Common:4; Rare:57 | ||||
| chr6:44127355-44127665 | Common:4; Rare:90 | ||||
| chr6:44246914-44247193 | Common:4; Rare:118 | ||||
| chr6:44257480-44257637 | Rare:42 | ||||
| chr6:44387449-44387749 | Common:4; Rare:79 |