Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:676346-676424 | Common:2; Rare:28 | ||||
chr19:676499-676668 | Common:3; Rare:66 | ||||
chr19:1103794-1104110 | Common:4; Rare:135 | ||||
chr19:1269068-1269343 | Common:2; Rare:103 | ||||
chr19:1275767-1276159 | Common:2; Rare:169 | ||||
chr19:2096052-2096415 | Common:1; Rare:117 | ||||
chr19:2096678-2097002 | Common:1; Rare:119 | ||||
chr19:2269433-2269721 | Common:3; Rare:132 | ||||
chr19:2328390-2328710 | Common:2; Rare:138 | ||||
chr19:2427868-2428205 | Common:4; Rare:99 | ||||
chr19:2433965-2434312 | Common:1; Rare:136; Clinvar:8; Clinvar (benign):3 | ||||
chr19:3186121-3186151 | Rare:10 | ||||
chr19:3981988-3982418 | Common:2; Rare:162; Clinvar:1; Clinvar (benign):5 | ||||
chr19:4182499-4182713 | Common:1; Rare:81; Clinvar:1 | ||||
chr19:4455251-4455623 | Common:1; Rare:84 |