Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:69398601-69398731 | Rare:33 | ||||
chr14:70417025-70417124 | Rare:25 | ||||
chr14:70600671-70600987 | Common:3; Rare:61 | ||||
chr14:73886815-73886859 | Rare:10 | ||||
chr14:73950062-73950312 | Common:6; Rare:102; Clinvar (benign):4 | ||||
chr14:74493568-74493777 | Common:3; Rare:78; Clinvar (benign):4 | ||||
chr14:74713082-74713198 | Rare:58 | ||||
chr14:75127001-75127120 | Rare:38 | ||||
chr14:75660825-75660962 | Rare:36 | ||||
chr14:77377082-77377410 | Common:1; Rare:89 | ||||
chr14:77457565-77457771 | Common:1; Rare:68 | ||||
chr14:77708011-77708131 | Common:1; Rare:58 | ||||
chr14:81220871-81221046 | Common:1; Rare:85 | ||||
chr14:92040031-92040164 | Common:2; Rare:31; Clinvar (benign):1 | ||||
chr14:92106578-92106789 | Common:2; Rare:61 |