| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34426000-34426203 | Common:5; Rare:85; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696717-34696972 | Common:1; Rare:57 | ||||
| chr6:36442806-36443087 | Common:2; Rare:101 | ||||
| chr6:36678463-36678766 | Common:1; Rare:79 | ||||
| chr6:37257635-37257792 | Rare:44 | ||||
| chr6:37353877-37354041 | Common:3; Rare:46 | ||||
| chr6:37433168-37433274 | Common:2; Rare:31 | ||||
| chr6:41921115-41921227 | Rare:28 | ||||
| chr6:42879577-42879937 | Rare:106 | ||||
| chr6:42929224-42929562 | Common:3; Rare:95 | ||||
| chr6:42984307-42984609 | Rare:75 | ||||
| chr6:43013841-43014270 | Common:2; Rare:104 | ||||
| chr6:43059812-43059892 | Rare:26 | ||||
| chr6:43516881-43517109 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576190 | Rare:95; Clinvar:4 |