EnhancerDB
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Enhancers that regulate LIN52[ENSG00000205659.6]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr14 74455865 74460935 enh51880 74551499 90564
Liver (HepG2) Large Intestine
chr14 74463545 74467695 enh92554 74551499 83804
Liver (HepG2)
chr14 74526685 74531110 enh15765 74551499 20389
Placenta Cervix (HeLa-S3) Lung (PC-9)
chr14 74598565 74604355 enh51881 74551499 47066
Liver (HepG2) Large Intestine Peripheral Blood (MM.1S) Neural Stem Cells (H9) Stomach
chr14 74605158 74613735 enh44033 74551499 53659
Liver (HepG2) Large Intestine Esophagus Thyroid Adrenal Muscle (Myotube)
chr14 74607211 74607609 vista18430 74551499 55712
VISTA
chr14 74625545 74632155 enh96533 74551499 74046
Peripheral Blood (MM.1S) Epithelial (MCF-7)
chr14 74636885 74644995 enh91040 74551499 85386
Bone Marrow (K562) Peripheral Blood (MM.1S)
Transcript facotrs that regulate LIN52[ENSG00000205659.6]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More
SNPs associated with LIN52[ENSG00000205659.6], confirmed by eQTL
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Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
Details of LIN52[ENSG00000205659.6]
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Genomic Location chr14:74551499-74667936[+]
TSS 74551499
Gene Name LIN52
Ensembl ID ENSG00000205659.6
ENTREZID 91750
Uniprot
Q52LA3
B3KN83
Protein Name
Protein lin-52 homolog
Expression levels of LIN52[ENSG00000205659.6]
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