| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42879577-42879950 | Rare:111 | ||||
| chr6:42890796-42890910 | Rare:42 | ||||
| chr6:42929105-42929175 | Rare:19 | ||||
| chr6:42929183-42929846 | Common:6; Rare:221 | ||||
| chr6:42984307-42984629 | Rare:81 | ||||
| chr6:43013838-43014270 | Common:2; Rare:106 | ||||
| chr6:43053824-43054033 | Common:1; Rare:56; Clinvar:5 | ||||
| chr6:43182105-43182233 | Rare:37 | ||||
| chr6:43427259-43427583 | Common:1; Rare:70 | ||||
| chr6:43427733-43427925 | Rare:52 | ||||
| chr6:43516785-43517123 | Common:6; Rare:122; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575903-43576234 | Common:2; Rare:135; Clinvar:8 | ||||
| chr6:43625507-43625795 | Rare:74 | ||||
| chr6:43626943-43627215 | Rare:40 | ||||
| chr6:43627287-43627488 | Rare:29 |