Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100825946-100826216 | Rare:65 | ||||
chr14:100829272-100829577 | Common:3; Rare:50 | ||||
chr14:100836225-100836289 | Rare:30 | ||||
chr14:100845471-100845524 | Rare:16 | ||||
chr14:101560025-101560052 | Rare:6 | ||||
chr14:101731299-101731414 | Common:3; Rare:27 | ||||
chr14:101948020-101948381 | Common:2; Rare:106 | ||||
chr14:103121374-103121487 | Rare:17 | ||||
chr14:103552102-103552439 | Common:3; Rare:81 | ||||
chr14:103694374-103694656 | Rare:55 | ||||
chr14:104718632-104718852 | Common:1; Rare:60; Clinvar (benign):3 | ||||
chr14:104815985-104816205 | Common:1; Rare:81 | ||||
chr14:105093915-105093948 | Rare:3 | ||||
chr14:105644660-105644690 | Rare:9 | ||||
chr14:105707502-105707826 | Common:2; Rare:91 |