| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:46129789-46130076 | Common:5; Rare:90 | ||||
| chr6:46652718-46653013 | Rare:74 | ||||
| chr6:46735331-46735740 | Common:3; Rare:108 | ||||
| chr6:46921865-46922080 | Common:2; Rare:57 | ||||
| chr6:47477695-47478047 | Common:2; Rare:86; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:49463167-49463407 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420161-52420349 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576944-52577292 | Common:6; Rare:119 | ||||
| chr6:52577347-52577478 | Common:1; Rare:41 | ||||
| chr6:52671054-52671171 | Rare:32 | ||||
| chr6:52995266-52995823 | Common:4; Rare:229 | ||||
| chr6:53061667-53061856 | Rare:45 | ||||
| chr6:53065151-53065608 | Common:1; Rare:141 | ||||
| chr6:53348816-53349222 | Common:2; Rare:171 | ||||
| chr6:53545098-53545203 | Rare:30 |