Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:23889368-23889556 | Common:1; Rare:63 | ||||
chr13:24512728-24512834 | Common:1; Rare:32 | ||||
chr13:24922801-24923090 | Common:2; Rare:94; Clinvar:1 | ||||
chr13:25287295-25287553 | Common:2; Rare:74 | ||||
chr13:25301492-25301712 | Common:1; Rare:83 | ||||
chr13:26221791-26221962 | Rare:49 | ||||
chr13:26222259-26222375 | Common:2; Rare:33 | ||||
chr13:27251234-27251617 | Common:8; Rare:118 | ||||
chr13:27424507-27424732 | Common:3; Rare:74 | ||||
chr13:27450130-27450222 | Common:3; Rare:28 | ||||
chr13:28138141-28138206 | Rare:17 | ||||
chr13:28659071-28659178 | Rare:46; Clinvar (pathogenic):1 | ||||
chr13:30306984-30307211 | Common:5; Rare:58 | ||||
chr13:30307410-30307605 | Common:2; Rare:65 | ||||
chr13:30464068-30464210 | Common:2; Rare:36 |