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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS047-08042
Organism
Homo sapiens
Tissue/cell
Fetal_placenta
Coordinate
chr12:56445480-56446140
Target genes
Number: 29
Name
Ensembl ID
BLOC1S1
ENSG00000135441
CD63
ENSG00000135404
SARNP
ENSG00000205323
ORMDL2
ENSG00000123353
RP11
ENSG00000257390
MMP19
ENSG00000123342
DGKA
ENSG00000065357
WIBG
ENSG00000170473
CDK2
ENSG00000123374
RAB5B
ENSG00000111540
AC034102.1
ENSG00000255990
SUOX
ENSG00000139531
RPS26
ENSG00000197728
PA2G4
ENSG00000170515
RPL41
ENSG00000229117
ZC3H10
ENSG00000135482
ESYT1
ENSG00000139641
MYL6B
ENSG00000196465
MYL6
ENSG00000092841
SMARCC2
ENSG00000139613
RNF41
ENSG00000181852
OBFC2B
ENSG00000139579
ANKRD52
ENSG00000139645
COQ10A
ENSG00000135469
CS
ENSG00000062485
CNPY2
ENSG00000257727
PAN2
ENSG00000135473
STAT2
ENSG00000170581
ATP5B
ENSG00000110955
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
TP53
MA0106.3
chr12:56445816-56445834
GACATGTCCGGGCACGGT
-
6.3
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr12
56445663
56445730
Enhancer Sequence
AAAAATTATT AAAGACTAAG ACATGGGCCG GGCGCAGTGC CTCACACCTG TAATCCCAGC 60
ACTTTGGGAG ACCAAGGTGG GTGGATTGCT TGAGGCCAGG AATTCGAGAG CAGCCTGGGC 120
AACATGGTGA AACCCTGTGT CTACTAAAGT ACAAAAAAAT AGCCAGGCAT GGTGGCACGC 180
ACCTGTCATC TCAGCTACTC GGGAGGCTGA AGCACAATAA TCGCTTGAAC CCAGGAGGCA 240
GAGGTTCCAG TGAGCCGAAA TGGCGCAACT GCACTCCAGC CTGGGTGACA AAGCAAAACT 300
CTGTCTCAAA AAATAAAAAA TAAAAATAAA AACTAAGACA TGTCCGGGCA CGGTAGCTCA 360
TGCCTATAAT CCCAGCACTT TGGGAAGGCC AGGATGGGAG GACTGCTTGA GTCCAGGAGT 420
TCAAGACCAG CCTGGGCAAC ATGGTGAAAC CCCTGTCTCT ACAAAAAAAA AAAAAAAAAA 480
AAAAAATAGC CAGGTATGGT AGCGTGTGCC TCTCTCGTCC CAGCTACTCG GAAGGGTAAG 540
GTGACAGGAT CGCTTGAGCC CAGAGGCAGA CATTACAGTG AGCTGAGATC ACACCAGTGC 600
ACTCCAGCTT GGGCAACAGA GGAAGACCTT TTCTCAAAAG AAAAGAAAAG AGGCCAGGCA 660