| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41072666-41072984 | Rare:90 | ||||
| chr6:41921104-41921237 | Rare:36 | ||||
| chr6:42050346-42050545 | Common:1; Rare:56 | ||||
| chr6:42142504-42142726 | Common:1; Rare:56 | ||||
| chr6:42746062-42746348 | Rare:84 | ||||
| chr6:42746835-42746996 | Rare:34 | ||||
| chr6:42879577-42879951 | Rare:112 | ||||
| chr6:42929209-42929594 | Common:4; Rare:116 | ||||
| chr6:42984322-42984619 | Rare:73 | ||||
| chr6:43013869-43014313 | Common:2; Rare:99 | ||||
| chr6:43076166-43076502 | Rare:114 | ||||
| chr6:43427298-43427576 | Common:1; Rare:54 | ||||
| chr6:43516858-43517112 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576185 | Rare:92; Clinvar:4 | ||||
| chr6:43770070-43770230 | Common:2; Rare:48 |