Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:24512728-24512844 | Common:3; Rare:34 | ||||
chr13:24922796-24923121 | Common:2; Rare:111; Clinvar:1 | ||||
chr13:25301492-25301706 | Common:1; Rare:82 | ||||
chr13:26221787-26221923 | Rare:34 | ||||
chr13:27251221-27251626 | Common:8; Rare:129 | ||||
chr13:27270730-27270830 | Rare:30 | ||||
chr13:27424509-27424824 | Common:2; Rare:104 | ||||
chr13:27449966-27450239 | Common:3; Rare:82 | ||||
chr13:27450346-27450644 | Common:4; Rare:112 | ||||
chr13:27620438-27620810 | Common:2; Rare:126 | ||||
chr13:28138096-28138229 | Common:1; Rare:46 | ||||
chr13:28495126-28495351 | Common:1; Rare:64 | ||||
chr13:28658942-28659194 | Rare:107; Clinvar (pathogenic):1 | ||||
chr13:28718797-28719126 | Common:1; Rare:82 | ||||
chr13:29428346-29428852 | Common:3; Rare:132 |