Enhancer ID: | E_01_121 | |
Enhancer symbol: | -- | |
Species: | Human | |
Position : | chr11:8301851-8303851 |
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Biosample name: | T-acute lymphoblastic leukemia (T-ALL) | |
Experiment class : | Low throughput |
Enhancer type: | Enhancer | |
Disease: | T-Cell leukemia | |
DO: | DOID:715 | |
Mesh: | D015458 | |
Distance from TSS: | >2KB | |
Pubmed ID: | 23302769 |
Enhancer experiment: | ChIP,RT-PCR,Luciferase Reporter Assay | |
Enhancer experiment description: | The LMO1 promoters display bivalent histone marks in multiple blood lineages including T-cells, and a 3’ flanking region at LMO1 þ 57 contains a transcriptional enhancer that is active in developing blood cells in transgenic mouse embryos. The LMO1 promoters become activated in T-ALL together with the 3’ enhancer, which is bound in primary T-ALL cells by SCL/TAL1 and GATA3. |
Target gene : | LMO1(RBTN1,RHOM1,TTG1) | |
Strong evidence: | -- | |
Less strong evidence: | ChIP,RT-PCR,Luciferase Reporter Assay | |
Target gene experiment description: | To investigate whether lack of expres_x0002_sion in the haematopoietic system may be due to active repression of the two LMO1 promoters, we analysed ChIP-Sequencing data released to the public domain by the NIH Roadmap Epigeno_x0002_mics Mapping Project. |
TF name : | TAL1(SCL,TCL5,bHLHa17,tal-1)GATA3(HDR,HDRS) | |
TF experiment: | ChIP,qPCR | |
TF experiment description: | ChIP assays on T-ALL cells from the same primagraft (X31) using antibodies against SCL/TAL1and GATA3. Analysis by quantitative PCR demonstrates significant binding of both SCL/TAL1 and GATA3 to the LMO1 +57 enhancer, with no binding to either of the two LMO1 promoters. |
Enhancer function : | -- |
Enhancer function experiment: | -- |
Enhancer function experiment description: |
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SNP ID: | -- | |
SNP position: | -- |
SNP experiment: | -- |
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