Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47426020-47426984 | Common:8; Rare:668 | ||||
chr11:47552303-47553460 | Common:23; Rare:1043 | ||||
chr11:47565286-47566749 | Common:39; Rare:822 | ||||
chr11:47578490-47578800 | Rare:80 | ||||
chr11:47578805-47579205 | Common:1; Rare:667; Clinvar:14; Clinvar (pathogenic):6 | ||||
chr11:47642095-47642216 | Rare:35 | ||||
chr11:47642404-47642902 | Rare:827 | ||||
chr11:47643108-47643880 | Rare:141 | ||||
chr11:47714644-47715606 | Common:8; Rare:381 | ||||
chr11:47765922-47766967 | Common:7; Rare:374 | ||||
chr11:47767101-47767834 | Common:17; Rare:1132 | ||||
chr11:47847691-47848091 | Rare:151 | ||||
chr11:47848261-47848477 | Common:3; Rare:373 | ||||
chr11:47848395-47848795 | Common:11; Rare:223 | ||||
chr11:47980191-47981051 | Common:9; Rare:535 |