Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:59176400-59176843 | Common:5; Rare:143 | ||||
chr10:59362489-59362705 | Common:1; Rare:59 | ||||
chr10:61662825-61662942 | Rare:29 | ||||
chr10:61901174-61901254 | Rare:21 | ||||
chr10:61901641-61901704 | Rare:17 | ||||
chr10:62268637-62268819 | Common:1; Rare:66 | ||||
chr10:62374236-62374449 | Common:1; Rare:56 | ||||
chr10:63133075-63133368 | Common:2; Rare:79 | ||||
chr10:63268791-63268903 | Common:1; Rare:27 | ||||
chr10:63269139-63269388 | Common:2; Rare:52 | ||||
chr10:63465940-63466074 | Rare:66 | ||||
chr10:63521153-63521489 | Common:7; Rare:117 | ||||
chr10:63521737-63522010 | Common:4; Rare:89 | ||||
chr10:68075189-68075466 | Common:4; Rare:119 | ||||
chr10:68231495-68231636 | Rare:57; Clinvar (pathogenic):2 |