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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-48728
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr9:131258420-131259100
Target genes
Number: 33
Name
Ensembl ID
AK1
ENSG00000106992
ST6GALNAC6
ENSG00000160408
ST6GALNAC4
ENSG00000136840
DPM2
ENSG00000136908
FAM102A
ENSG00000167106
SLC25A25
ENSG00000148339
NAIF1
ENSG00000171169
AL590708.2
ENSG00000232850
PTGES2
ENSG00000148334
C9orf16
ENSG00000171159
DNM1
ENSG00000106976
CIZ1
ENSG00000148337
SWI5
ENSG00000175854
GOLGA2
ENSG00000167110
COQ4
ENSG00000167113
TRUB2
ENSG00000167112
SLC27A4
ENSG00000167114
TMSB4XP4
ENSG00000223551
URM1
ENSG00000167118
CERCAM
ENSG00000167123
RP11
ENSG00000228510
ODF2
ENSG00000136811
GLE1
ENSG00000119392
SPTAN1
ENSG00000197694
WDR34
ENSG00000119333
SET
ENSG00000119335
PKN3
ENSG00000160447
ZDHHC12
ENSG00000160446
ZER1
ENSG00000160445
TBC1D13
ENSG00000107021
ENDOG
ENSG00000167136
C9orf114
ENSG00000198917
LRRC8A
ENSG00000136802
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr9
131258779
131258899
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH09I128493
chr9
131255794
131258830
Enhancer Sequence
GTTAGAGGCA CTTGGTCCCA TCTCTGTCCT CTTCCTAGGA CCTGAGACTT TCAGCCACTT 60
AGCTGTTTTT TGCTTAGTGT GCGGAAGTGT TGAGGGACTC GAGGCCCTGG AAGGTACTAG 120
GCAGACCTCA GAGGAAAAGC TGCTTCCATT TCAGTGGTAA GCATTGTGGG AGAGAGCAAG 180
GGGGCCTCTC AGCCTGGGGA GACACTCCAT GACAGCATGA TCAGGATCTG CCCACCTGTA 240
GGCACCACCT GTCCCAAAAG GCATGCCTGG TCCAGGCCTG CCAGGAGGGC CCAGTTTGAA 300
TGGAGCAGCC AGTATACTGT GGTGGGGGCA CTTCCCCACT CTTTTCTGCC CTTTCTTGCC 360
AGTCACCCTT CCCAAGACCT TTCTGATCTG ACCGTTCTCT GTTATTTACG GATTGTTGGA 420
GGCAGTCAGA GGTGAAGGGT ACGGCTTTGG GAATCAGAAG CCCTGGCCTT GGGGCCCAGC 480
TCTGCCACTT ACCAGCATTG TGATCTTGAG CAAATCATTT AATTCCTTTG AAGCTCAATT 540
TCCTCCTTTT GAGGAAAGGG TCAAGGTAGA GTTTATCTAT CTATCTATCT ATCTATCTAT 600
CATCTATCTA TCATGTCACT CTGTCACCCA GGCTGGAGTG CAGTGGTGCA ATCTCAGCTC 660
ACTGCAACCT CGACCTCCTG 680