| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013857-43014329 | Common:2; Rare:108 | ||||
| chr6:43014441-43014540 | Common:3; Rare:28 | ||||
| chr6:43014731-43014974 | Rare:41 | ||||
| chr6:43040772-43040782 | Rare:3 | ||||
| chr6:43053699-43054011 | Common:2; Rare:115; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059808-43059948 | Common:1; Rare:43 | ||||
| chr6:43076166-43076492 | Rare:108 | ||||
| chr6:43076525-43076916 | Common:3; Rare:87 | ||||
| chr6:43130641-43130818 | Rare:39 | ||||
| chr6:43144278-43144606 | Common:3; Rare:95 | ||||
| chr6:43170671-43170919 | Rare:44 | ||||
| chr6:43171055-43171536 | Rare:144 | ||||
| chr6:43182029-43182239 | Common:1; Rare:60 | ||||
| chr6:43226358-43226511 | Common:1; Rare:31 | ||||
| chr6:43427775-43427954 | Rare:54 |