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Items: 4

1.

HIC2 represses BCL11A transcription to regulate hemoglobin switching during development (ATAC-Seq)

(Submitter supplied) The switch from fetal to adult hemoglobin production has been studied in great depth in part because of its relevance to the treatment of hemolobinopathies. Transcription factor BCL11A, which is essential for repression of the fetal beta-type globin (γ-globin) genes after birth, is largely controlled at the level of transcription but the mechanism of BCL11A developmental control is unknown. Here, using a CRISPR-Cas9 screen in human erythroblasts, we identify transcription factor HIC2 as a repressor of BCL11A transcription. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL30173
12 Samples
Download data: BIGWIG
Series
Accession:
GSE173582
ID:
200173582
2.

HIC2 represses BCL11A transcription to regulate hemoglobin switching during development

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by array; Other
Platforms:
GPL30172 GPL30173
65 Samples
Download data: BED, BIGWIG, TSV
Series
Accession:
GSE173587
ID:
200173587
3.

NextSeq 2000 (Homo sapiens)

Platform
Accession:
GPL30173
ID:
100030173
4.

Adult erythroblasts rep1

Organism:
Homo sapiens
Source name:
Adult erythroblasts
Platform:
GPL30173
Series:
GSE173582 GSE173587
Download data: BIGWIG
Sample
Accession:
GSM5530943
ID:
305530943
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