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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-48685
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr9:130576360-130577290
Target genes
Number: 35
Name
Ensembl ID
SLC2A8
ENSG00000136856
ZNF79
ENSG00000196152
SNORA65
ENSG00000201302
RPL12
ENSG00000197958
LRSAM1
ENSG00000148356
Y
ENSG00000200788
FAM129B
ENSG00000136830
STXBP1
ENSG00000136854
C9orf117
ENSG00000160401
RP11
ENSG00000248666
TTC16
ENSG00000167094
PTRH1
ENSG00000187024
TOR2A
ENSG00000160404
SH2D3C
ENSG00000095370
CDK9
ENSG00000136807
FPGS
ENSG00000136877
ENG
ENSG00000106991
AK1
ENSG00000106992
ST6GALNAC6
ENSG00000160408
ST6GALNAC4
ENSG00000136840
PIP5KL1
ENSG00000167103
DPM2
ENSG00000136908
FAM102A
ENSG00000167106
SLC25A25
ENSG00000148339
NAIF1
ENSG00000171169
AL590708.2
ENSG00000232850
PTGES2
ENSG00000148334
LCN2
ENSG00000148346
C9orf16
ENSG00000171159
DNM1
ENSG00000106976
CIZ1
ENSG00000148337
GOLGA2
ENSG00000167110
TRUB2
ENSG00000167112
SLC27A4
ENSG00000167114
URM1
ENSG00000167118
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
Nr2f6(var.2)
MA0728.1
chr9:130576707-130576722
GAGGTCAAGAGGTCG
+
7.26
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr9
130576705
130576779
Enhancer Sequence
CCCTTGACCC CCTGCTCCCT CAGCAGAGAC GGAGGGAGGG GCTGCTGGTG GTCAGGGACC 60
TGCACTGTGT AGAGGGAGCC TGGCTGTGTG GCCTGGAACA AGTCCCTCCC TCCCTGTGCG 120
CCTCAGGTGG CCTGTCTGTG AGATGAGAAG AAGACCAGAC TGAAGCCTGT TCACCATATG 180
CCAGGCAGTG CTTTCTGCAG ACCCCCTTGC AGAGACCTTG TGATGGAGAA TTATACACAT 240
TTGACAGACG AGGGAACTGT GGCTGGTTTC AAGAAGCCAT GGAGGCCGGG CACGGTGGCT 300
CACGCCTGTA ATCCCAGCAC TTTGGGAGGC TGAGGCGGGC GGATCATGAG GTCAAGAGGT 360
CGAGACCATC TGGCCAACAT GGTGAAACCC CGTCTCTGCT AAAAATACAA AAATTATTAG 420
CTGGACGTGG TGGCGCATGC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGACAATT 480
GCTTGAACCT GGGAGGCAGA GGTTGCAGTG AGCTGAGATA GAGATAGTGC CACTGTACTC 540
CAGCCTGGGC GACAGAGCAA GACTCCATCT CAAAAAAAAA AAAGCCATGG GACCTGCCTA 600
CAGTCACAGG CCAACAAGGT GGCAGGTCCA GGATTTGAAC TTAGAGCAGT CGAGGGCCTG 660
TGTTCGGAAC CCCAGAGTGA GAGTGTGGAT GGGGCCTCCT GGTGTTTGCT TTCTTGCAGC 720
CTAGACCCTG GGGTGTGCTG TCGAGTGGGT GAATGGCAGA GGGGAACTGG CTGAATGAAA 780
ACCTGCTGTG CCCTGGATGC TGCTACTGTT CAGGATGCCA CCCCTGCCAC CAGGCCAGCC 840
CAGTGGGGGC CAACTACAAA AGCAGCCCTG TCCTGTGCCC TCACCCCACC CTGGCTTTGA 900
ATGTCACTGC CCTTCTCCCA GCCCAACCCA 930