| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:50821521-50821721 | Common:1; Rare:37 | ||||
| chr6:50821904-50822047 | Common:3; Rare:17 | ||||
| chr6:52420150-52420378 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671054-52671167 | Rare:30 | ||||
| chr6:52995275-52995833 | Common:4; Rare:227 | ||||
| chr6:53065581-53065614 | Rare:8 | ||||
| chr6:53348858-53349222 | Common:2; Rare:148 | ||||
| chr6:54846574-54846820 | Common:1; Rare:61 | ||||
| chr6:55579129-55579276 | Common:1; Rare:55 | ||||
| chr6:56542795-56543014 | Common:2; Rare:37 | ||||
| chr6:57089973-57090227 | Rare:101 | ||||
| chr6:63572190-63572587 | Rare:143 | ||||
| chr6:63635747-63635999 | Common:1; Rare:85 | ||||
| chr6:69796847-69797146 | Common:1; Rare:93; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:70413222-70413605 | Common:2; Rare:108 |