| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52576992-52577317 | Common:6; Rare:119 | ||||
| chr6:52671031-52671167 | Rare:39 | ||||
| chr6:52995275-52995819 | Common:4; Rare:225 | ||||
| chr6:53065374-53065604 | Common:1; Rare:71 | ||||
| chr6:53348847-53349242 | Common:2; Rare:162 | ||||
| chr6:53665648-53665937 | Common:2; Rare:60 | ||||
| chr6:54846251-54846332 | Common:4; Rare:16 | ||||
| chr6:54846379-54846799 | Common:2; Rare:109 | ||||
| chr6:56542790-56543004 | Common:1; Rare:37 | ||||
| chr6:56851808-56852028 | Rare:39 | ||||
| chr6:57172134-57172319 | Rare:50 | ||||
| chr6:57172547-57172764 | Common:1; Rare:72 | ||||
| chr6:63572193-63572497 | Rare:109 | ||||
| chr6:69796847-69797112 | Rare:88; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:70283180-70283317 | Rare:26 |