EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-09303 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr12:7242840-7244040 
Target genes
Number: 42             
NameEnsembl ID
NCAPD2ENSG00000010292
MRPL51ENSG00000111639
SCARNA10ENSG00000256329
GAPDHENSG00000111640
CHD4ENSG00000111642
C12orf53ENSG00000139200
COPS7AENSG00000111652
PTMSENSG00000159335
MLF2ENSG00000089693
LAG3ENSG00000089692
AC125494.2ENSG00000244532
CD4ENSG00000010610
GPR162ENSG00000250510
U47924.11ENSG00000256010
LEPREL2ENSG00000110811
GNB3ENSG00000111664
CDCA3ENSG00000111665
USP5ENSG00000111667
TPI1ENSG00000111669
RPL13P5ENSG00000240370
LRRC23ENSG00000010626
SPSB2ENSG00000111671
ENO2ENSG00000111674
ATN1ENSG00000111676
C12orf57ENSG00000111678
PTPN6ENSG00000111679
SCARNA12ENSG00000238795
EMG1ENSG00000126749
PHB2ENSG00000215021
U47924.19ENSG00000255896
C1SENSG00000182326
LPCAT3ENSG00000111684
RP3ENSG00000239701
C1RENSG00000159403
ABC12ENSG00000205885
C1RLENSG00000139178
U6ENSG00000200345
RBP5ENSG00000139194
CLSTN3ENSG00000139182
RP11ENSG00000256967
PEX5ENSG00000139197
ACSM4ENSG00000215009
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1272429227243105
Enhancer Sequence
AGATCTGGTG GAAGAAGGAC AGGGGGTAGG AAGAAGATCT GTTGCGGAGT GGCGCACGTG 60
GTGGCTCAGT GATGGTCCTC CTTGTCTCGC CCAGAGTGCA TCATGCACCA CAATGGCTCT 120
GGCTGGTCAC TACCTGCTGG GCTCAGCTGC TGCAAACTTC CCCATGTGAC TTTCAGCTGT 180
TCCCTGAGTC TCCCACTGAC TCACTCTTTG CGTGTTGTCC TGGACTGGGT ACCTCACCCT 240
TTCCCTGTTT TCTGCTCCTC TGGCAGGTTT CAGGTCCTTC TCCATCCCCA CCACCTCCTA 300
TGGCCTGTTC CCCTGGGGTC CTGGTTGTCT GTACCCAGCC TTTACCTGCC CCTCATTCCC 360
AGAGCTCAGA CAGCTCCGCT TTATTTTCTG TCTTCAGATT CCACCTCAGC CTAATCAAAC 420
CATTCACACC TCGAGTGCCT CCTGATGCCC TCGGCGGAAC ATGAGCCCTG AAGCCCACCC 480
ATCTCAGTGT CAGCAGGCAC TGCCTCGTCC CTCTTCCTTC CTCCTCACAG CCTCCTCAAC 540
CTCTCCTTGA CTCTGCCAGC AAACGCCCTC CCCCAACACT GCACACTCGC CAAGTCTTCT 600
GAGCCGGTAA GACGTGCCAT TGTCATGTAA TTCACGCATA ATCTCCAGGG GTCTCCTGGG 660
AATGGTAGTT GTTGGACCTT CGCAGGCTCT GCTTGAGCCC TGAATCTCAT TTTTACTGGA 720
TAGAGAAAGA CAGGCCTGGG AAGGTACCCT TGGTTGCCAC AGAGGTGAGG GTTCTGAGCA 780
CACTGTCCTT GCTGAAGGCT ATTCCTGTGC TGCCAGAGCC CACATTTCTC CTCCTCATGT 840
CCCTGTGTTC CTGTTGAAGC AGGCAGCCAT GTCAATCATT TCCTTGGAGA CAGGGAAGCT 900
GAGGCACAGT GGTTTCCCAA AGACTCTCAG CTAGACAGCA GATGGGGAAG GTTTTCCTGA 960
CTCAGTGGAT GTTGAATTTC CTGAGTGGGT CCTGTCCCCT TCCTTCTCTG TGCTTCTCCC 1020
CTCAGTGCTC ACCGAGGGCC TCTACACCAG TGAGCGCCCA TCCAGGGCAT CCCCGGGCTC 1080
TCAGAGAGGC CGTTGGCCAT CAGCTCTTGT GGGGCTGGGC TGTGTCTGGG GGTGTGCATG 1140
CCATACAGAT CCCAGATCCC AGAGGGCCCA GTTTTGTCTC CCCTCTGCCC GCCCATCCTG 1200