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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-08865
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr11:118896790-118897310
Target genes
Number: 24
Name
Ensembl ID
DDX6
ENSG00000110367
UPK2
ENSG00000110375
BCL9L
ENSG00000186174
AP004609.1
ENSG00000239726
AP003392.1
ENSG00000242712
RP11
ENSG00000255121
CCDC84
ENSG00000186166
RPL23AP64
ENSG00000240970
TRAPPC4
ENSG00000196655
RPS25
ENSG00000118181
SLC37A4
ENSG00000137700
HYOU1
ENSG00000149428
VPS11
ENSG00000160695
HMBS
ENSG00000256269
H2AFX
ENSG00000188486
C2CD2L
ENSG00000172375
DPAGT1
ENSG00000172269
HINFP
ENSG00000172273
NLRX1
ENSG00000160703
PDZD3
ENSG00000172367
CBL
ENSG00000110395
MCAM
ENSG00000076706
RNF26
ENSG00000173456
C1QTNF5
ENSG00000223953
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr11
118896870
118897061
Enhancer Sequence
CTATGGATAC AGTCCCGGCA ATGTCACGTC CTCAGAACAG GGCAGAGAAC ACCCACCCCT 60
GGACTCTGAC ACAGCAGGGC CTCTGCTGAC GGGTCTTTGG CAATCCCACC ACAGTTCTTG 120
GCCCTGGGCA GCTCTGGGAG GCCCTGGGAC CTGCTCATTA CATTCTGAGG CCAAACTCTA 180
CAACATCCCC TCCTCCCCCG TCAGGCAGGA CTAGGACACG TGCTGGGGAG GGCACCTAGT 240
CTGTTCCCAG CCCATTTTCC TGGGGCTGTG GAGCAACCTA CAGCTAAGCT AAGAAATATT 300
CTGGCTGTCC TTCACATCAG TTAAAACTCT ACCCAAGAGC CTTACTTCCA CAACCGTAGG 360
AAAGCTAAGA CCAGCCTGGA ATCATTCCCT CTTCACCCGG TCTAAACCAG CAGATGCCAA 420
CCTGCCTGTG CCCTGGGACT CCCATCTCTC CAGTGCCTGT CCCAGCCACG CCGTGAAGAC 480
TGAAAGGGAC CCTTCTCCTT CCTGTCCCTT CTGCCCGCTC 520