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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS018-11812
Organism
Homo sapiens
Tissue/cell
CD19+
Coordinate
chr19:58570680-58571330
Target genes
Number: 26
Name
Ensembl ID
ZNF134
ENSG00000213762
ZNF776
ENSG00000152443
ZNF586
ENSG00000083828
ZNF552
ENSG00000178935
ZNF587
ENSG00000198466
ZNF256
ENSG00000152454
CTD
ENSG00000243234
C19orf18
ENSG00000177025
VN2R19P
ENSG00000235974
ZNF135
ENSG00000176293
AC008751.2
ENSG00000243642
ZSCAN18
ENSG00000121413
ZNF329
ENSG00000181894
ZNF274
ENSG00000171606
ZNF544
ENSG00000198131
AC020915.4
ENSG00000142396
RPS5
ENSG00000083845
AC012313.1
ENSG00000232098
ZNF132
ENSG00000131849
ZNF324B
ENSG00000249471
ZNF324
ENSG00000083812
ZNF446
ENSG00000083838
ZBTB45
ENSG00000119574
TRIM28
ENSG00000130726
CHMP2A
ENSG00000130724
UBE2M
ENSG00000130725
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
KLF5
MA0599.1
chr19:58570950-58570960
GCCCCGCCCC
+
6.02
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2
Chromosome
Start
End
chr19
58570713
58571200
chr19
58571200
58571210
Enhancer Sequence
GAGCTAGGCC GGCGAGGAGG GGGAGGGGAG GCCAGGCCGG GCCGGGCCGG GCCGGGTGCG 60
GGGGGTCCGG GGATCTTCCT GAGGCCCTGG CGGGGCGAGT TTCCAGCAGC GCGCGTCTGT 120
GTGGAGTCCG TTTTGCTGCC CGGGGCCTGG GGAAGGCCGT TTCGGGGCTG GCGGGGGCAG 180
GCTTTGCGGG GCATCCCTAG TCTGAGAGGA GGGCGGGGCC CAACGCCCAG CTGGACAGGA 240
GCTGCTCCGA CGGCCCCTGA GGGAACGCGC GCCCCGCCCC TGGCCCCACC TCTGCCCCAC 300
ACCGGGCACT GGGCCGCCAC CTTTGTTGAT GGAAGAGAGA AACTGAGGCA TAGTGCCCAG 360
GGCCAGGGGA CCGCAACCAC CCGGCCCTTG TCACTGTAGC GTTAAGGCTC AGAGTCTGCG 420
CAGCAGATAT GTGTCCGCAC CCGCCAGGCC TTCAGCTTCC CTCAGACAGG CGGGAAAACC 480
CTAGGCTGCC CTTCTCCGAG CGGAGGGCCG CCCCACACAC AGCAGGCGCT TAAACGGGTA 540
CGCGGGGCCC TGGACGGCTC TCCGCGGAGC TCCCCAGGCT CTGGCGCAGT TCCCCGGCTT 600
GGGGACCTGA GCACCGCCTC TGCCTGCCCC AGCTGCTCAC CTCCCCTTTC 650