Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:44230426-44230618 | Rare:61 | ||||
chr6:44249668-44250079 | Common:3; Rare:131 | ||||
chr6:44250489-44250852 | Common:2; Rare:88 | ||||
chr6:44251095-44251426 | Common:2; Rare:102 | ||||
chr6:44251436-44251884 | Rare:154 | ||||
chr6:44253174-44253673 | Common:7; Rare:194 | ||||
chr6:45303374-45303663 | Rare:52 | ||||
chr6:47606249-47606534 | Common:1; Rare:70; Clinvar (benign):1 | ||||
chr6:48073539-48073618 | Rare:9 | ||||
chr6:49358265-49358548 | Rare:55 | ||||
chr6:52267770-52267995 | Common:1; Rare:65 | ||||
chr6:52420946-52421025 | Rare:18 | ||||
chr6:52664224-52664503 | Common:4; Rare:86 | ||||
chr6:53292250-53292367 | Common:1; Rare:25 | ||||
chr6:53348015-53348153 | Common:1; Rare:39 |