Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102139650-102139926 | Rare:95 | ||||
chr14:102305118-102305287 | Common:1; Rare:57 | ||||
chr14:102362847-102363094 | Rare:112 | ||||
chr14:103123266-103123481 | Rare:37 | ||||
chr14:103333862-103334252 | Common:3; Rare:160 | ||||
chr14:103529081-103529243 | Common:1; Rare:50 | ||||
chr14:103562623-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
chr14:103629359-103629451 | Common:2; Rare:35 | ||||
chr14:104776661-104776975 | Common:1; Rare:74; Clinvar:4; Clinvar (benign):4 | ||||
chr15:25438984-25439158 | Common:2; Rare:65 | ||||
chr15:25862500-25862571 | Rare:9 | ||||
chr15:28099299-28099518 | Common:2; Rare:78; Clinvar:1 | ||||
chr15:29269791-29269877 | Rare:32 | ||||
chr15:31870646-31870951 | Rare:98 | ||||
chr15:32615112-32615566 | Common:6; Rare:117 |