Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101244750-101245070 | Common:3; Rare:59 | ||||
chr10:101297976-101298117 | Common:1; Rare:23 | ||||
chr10:101569862-101569977 | Rare:29 | ||||
chr10:101693757-101693891 | Common:1; Rare:22 | ||||
chr10:101694076-101694444 | Rare:85; Clinvar:1 | ||||
chr10:102054053-102054297 | Rare:43 | ||||
chr10:102072874-102073274 | Common:4; Rare:110 | ||||
chr10:102117767-102118167 | Common:4; Rare:143 | ||||
chr10:102119413-102119530 | Rare:16 | ||||
chr10:102119643-102119889 | Common:1; Rare:46 | ||||
chr10:102127953-102128353 | Common:5; Rare:84 | ||||
chr10:102133553-102133806 | Common:1; Rare:58 | ||||
chr10:102169581-102169766 | Common:1; Rare:56 | ||||
chr10:102230023-102230428 | Common:2; Rare:132 | ||||
chr10:102230436-102230857 | Rare:148; Clinvar (pathogenic):1 |