Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:24922790-24923121 | Common:2; Rare:115; Clinvar:1 | ||||
chr13:25287259-25287562 | Common:2; Rare:96 | ||||
chr13:26221786-26221983 | Rare:58 | ||||
chr13:26222235-26222375 | Common:3; Rare:38 | ||||
chr13:27251235-27251626 | Common:8; Rare:121 | ||||
chr13:27270702-27270889 | Rare:72 | ||||
chr13:27424514-27424762 | Common:2; Rare:82 | ||||
chr13:27450094-27450240 | Common:3; Rare:49 | ||||
chr13:27450346-27450643 | Common:4; Rare:112 | ||||
chr13:27620390-27620810 | Common:3; Rare:143 | ||||
chr13:27621090-27621192 | Common:1; Rare:26 | ||||
chr13:28138142-28138229 | Common:1; Rare:25 | ||||
chr13:28658857-28659001 | Common:1; Rare:30 | ||||
chr13:28659052-28659194 | Rare:60; Clinvar (pathogenic):1 | ||||
chr13:29595631-29595915 | Common:2; Rare:100 |