Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102362849-102363092 | Rare:111 | ||||
chr14:103123331-103123462 | Rare:22 | ||||
chr14:103529026-103529246 | Common:1; Rare:66 | ||||
chr14:103562634-103563002 | Common:5; Rare:128; Clinvar (benign):1 | ||||
chr14:103715426-103715896 | Common:1; Rare:158 | ||||
chr14:105248445-105248628 | Common:4; Rare:90 | ||||
chr15:34101840-34102080 | Common:1; Rare:49 | ||||
chr15:37099178-37099353 | Rare:45 | ||||
chr15:37100207-37100448 | Rare:50 | ||||
chr15:37100510-37100678 | Common:1; Rare:48 | ||||
chr15:40039094-40039311 | Rare:90 | ||||
chr15:40160911-40161115 | Common:3; Rare:47 | ||||
chr15:40695100-40695207 | Rare:29 | ||||
chr15:40807450-40807767 | Common:4; Rare:106 | ||||
chr15:40953218-40953475 | Common:1; Rare:70 |