| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:49463157-49463412 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420122-52420356 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576987-52577307 | Common:6; Rare:120 | ||||
| chr6:52671031-52671183 | Rare:46 | ||||
| chr6:52995267-52995833 | Common:4; Rare:230 | ||||
| chr6:53065354-53065672 | Common:1; Rare:90 | ||||
| chr6:53348871-53349272 | Common:2; Rare:147 | ||||
| chr6:56542785-56543014 | Common:2; Rare:41 | ||||
| chr6:56843077-56843337 | Common:1; Rare:76 | ||||
| chr6:56843453-56843779 | Common:8; Rare:78 | ||||
| chr6:57172533-57172760 | Common:1; Rare:74 | ||||
| chr6:57317529-57317647 | Rare:30 | ||||
| chr6:63572448-63572560 | Rare:41 | ||||
| chr6:68634930-68635361 | Common:2; Rare:118 | ||||
| chr6:68635716-68635967 | Rare:48 |