| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32838718-32838912 | Common:6; Rare:35 | ||||
| chr6:32844001-32844087 | Rare:24; Clinvar:1 | ||||
| chr6:32854010-32854216 | Common:2; Rare:50 | ||||
| chr6:33200656-33200925 | Common:2; Rare:82 | ||||
| chr6:33271650-33272131 | Common:3; Rare:171 | ||||
| chr6:33289175-33289640 | Common:4; Rare:106 | ||||
| chr6:33298943-33299070 | Rare:31 | ||||
| chr6:33418039-33418508 | Common:3; Rare:110 | ||||
| chr6:33420043-33420267 | Rare:48 | ||||
| chr6:33454406-33454588 | Rare:50 | ||||
| chr6:34236752-34236914 | Common:2; Rare:64 | ||||
| chr6:34426000-34426173 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696738-34696988 | Common:1; Rare:60 | ||||
| chr6:34757285-34757550 | Common:2; Rare:73 | ||||
| chr6:34887964-34888145 | Common:1; Rare:40 |