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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS040-17421
Organism
Homo sapiens
Tissue/cell
Esophagus
Coordinate
chr19:1093260-1093900
Target genes
Number: 31
Name
Ensembl ID
WDR18
ENSG00000065268
RNF126
ENSG00000070423
FSTL3
ENSG00000070404
PALM
ENSG00000099864
ARID3A
ENSG00000116017
KISS1R
ENSG00000116014
R3HDM4
ENSG00000198858
MED16
ENSG00000175221
PTBP1
ENSG00000011304
CFD
ENSG00000197766
TPGS1
ENSG00000141933
BSG
ENSG00000172270
C19orf6
ENSG00000182087
CNN2
ENSG00000064666
ABCA7
ENSG00000064687
HMHA1
ENSG00000180448
POLR2E
ENSG00000099817
GPX4
ENSG00000167468
SBNO2
ENSG00000064932
STK11
ENSG00000118046
C19orf26
ENSG00000099625
ATP5D
ENSG00000099624
MIDN
ENSG00000167470
CIRBP
ENSG00000099622
C19orf24
ENSG00000228300
MUM1
ENSG00000160953
EFNA2
ENSG00000099617
NDUFS7
ENSG00000115286
AC005329.7
ENSG00000248015
DAZAP1
ENSG00000071626
REEP6
ENSG00000115255
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
NR2C2
MA0504.1
chr19:1093725-1093740
AGGGGTCAGAGATCA
+
6.31
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr19
1093635
1093780
Enhancer Sequence
CCACTGATTA ATTCTGGGCG TGGGGCTGCG CCCCTAAGGC GCTTGCAATC CCCCAACCGC 60
TGAGGGCTTT AGAGCCATAC TAGGGAGGCA GACAGGTGCG GAGACTTCCG CAAAGCAGGT 120
GCTGAAACCG AGGGTCCCAG GGGTCCTGGG AAAAGAGGCC CGAGCACAAG CTCGAGGGAC 180
GAGTACCGGA CGCTGACAGG GGAGAGGGGG CATGGGGTGC GGAGGAATGG GCTGGGGCGG 240
GCAGGGGCCG CAGCTCACAA GGAGGCTGCG CTGACCCAGA CGGGGCCTCC TGGGCCAGGC 300
CAAGAAGCTG GAAGTGCACC CAACGGCCAG GATGGGGGAG CCAAGGGACA CTAGGGCAAA 360
GGACATGGGG GGCTGGGGGT GAGTGGGGAG GCCCTTGTGA CTCTCCTCGT TGGCAGGAAG 420
AGAGAAGGGG ACTGAGAGGG AAACTAGAAA GAAGCTGAGC ATGAGAGGGG TCAGAGATCA 480
ACGGCATCAC CCACAGCAAG GAAGGGGAGG GGAGTTTTCC TCCCAGACTG GGCAGAGAGA 540
CAAATGCTGG GCACCAGGCG AGTGGGGGTG GGTGCTAGCG ACCGGCTCCT CGGCAGGTGC 600
TCTGGTGGCT TCACCGGAAC TCCCCCGGGA CCCGCTGCTC 640