Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102362847-102363119 | Rare:117 | ||||
chr14:103333951-103334252 | Common:2; Rare:123 | ||||
chr14:103529022-103529233 | Common:1; Rare:64 | ||||
chr14:103562620-103563035 | Common:7; Rare:158; Clinvar (benign):3 | ||||
chr14:103715397-103715851 | Common:1; Rare:156 | ||||
chr14:105248457-105248602 | Common:4; Rare:69 | ||||
chr14:105419753-105419882 | Rare:26 | ||||
chr15:22838370-22838759 | Common:3; Rare:142 | ||||
chr15:25438977-25439227 | Common:3; Rare:96 | ||||
chr15:34101848-34102073 | Common:1; Rare:45 | ||||
chr15:34588444-34588565 | Rare:35 | ||||
chr15:40039094-40039348 | Rare:100 | ||||
chr15:40160896-40161102 | Common:2; Rare:51 | ||||
chr15:40695094-40695227 | Common:2; Rare:41 | ||||
chr15:40807053-40807127 | Rare:20 |