| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44223468-44223805 | Common:2; Rare:101 | ||||
| chr6:44246914-44247184 | Common:4; Rare:113 | ||||
| chr6:44270731-44270875 | Rare:36 | ||||
| chr6:44313313-44313527 | Common:1; Rare:56; Clinvar (benign):2 | ||||
| chr6:44387438-44387738 | Common:4; Rare:77 | ||||
| chr6:45377643-45377741 | Common:1; Rare:38 | ||||
| chr6:45377866-45378142 | Common:2; Rare:95 | ||||
| chr6:46129793-46130176 | Common:5; Rare:122 | ||||
| chr6:46652718-46653022 | Rare:75 | ||||
| chr6:47477636-47478006 | Common:2; Rare:97; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:47478100-47478232 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:48068808-48068944 | Common:1; Rare:39 | ||||
| chr6:49463141-49463431 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284756-52285088 | Common:2; Rare:98 | ||||
| chr6:52420108-52420386 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):2 |