| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5260737-5261051 | Common:4; Rare:108; Clinvar (benign):2 | ||||
| chr6:10694809-10694973 | Common:3; Rare:54 | ||||
| chr6:10747582-10747860 | Common:3; Rare:107 | ||||
| chr6:13615211-13615439 | Common:2; Rare:98 | ||||
| chr6:24666798-24667176 | Common:2; Rare:163 | ||||
| chr6:26123771-26124263 | Common:6; Rare:245 | ||||
| chr6:26197276-26197436 | Common:1; Rare:60 | ||||
| chr6:26199290-26199586 | Common:2; Rare:129 | ||||
| chr6:26204471-26204633 | Common:1; Rare:81 | ||||
| chr6:26216654-26216933 | Rare:108 | ||||
| chr6:26251375-26251640 | Rare:78 | ||||
| chr6:26271389-26271579 | Common:2; Rare:53 | ||||
| chr6:26272635-26272972 | Common:2; Rare:91 | ||||
| chr6:26538297-26538432 | Common:1; Rare:25 | ||||
| chr6:27132756-27133053 | Common:3; Rare:123 |