EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-28921 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr2:218753400-218755680 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs116819734chr2218753780hg19
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESRRBMA0141.3chr2:218753742-218753753TCAAGGTCAAA+6.14
EsrraMA0592.2chr2:218753741-218753752TTCAAGGTCAA+6.14
HNF4GMA0484.1chr2:218753743-218753758CAAGGTCAAAGGCCA+6.45
KLF14MA0740.1chr2:218754811-218754825GGCCACGCCCCCTC+7.52
KLF16MA0741.1chr2:218754812-218754823GCCACGCCCCC+6.62
NR2C2MA0504.1chr2:218753743-218753758CAAGGTCAAAGGCCA+6.18
Nr2f6MA0677.1chr2:218753744-218753758AAGGTCAAAGGCCA+6.44
RxraMA0512.2chr2:218753744-218753758AAGGTCAAAGGCCA+6.09
SP1MA0079.4chr2:218754809-218754824ATGGCCACGCCCCCT+6.91
SP3MA0746.2chr2:218754811-218754824GGCCACGCCCCCT+6.82
SP4MA0685.1chr2:218754809-218754826ATGGCCACGCCCCCTCC+7.42
SP8MA0747.1chr2:218754812-218754824GCCACGCCCCCT+6.92
ZIC1MA0696.1chr2:218755298-218755312CACAGCAGGGGGCA-6.83
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_00005chr2:218749169-218810848Adipose_Nuclei
SE_00853chr2:218755216-218756366Adrenal_Gland
SE_01533chr2:218753600-218756995Aorta
SE_05119chr2:218754638-218756563Brain_Cingulate_Gyrus
SE_05795chr2:218750061-218754542Brain_Hippocampus_Middle
SE_05795chr2:218754777-218756736Brain_Hippocampus_Middle
SE_26522chr2:218754400-218755238Esophagus
SE_26522chr2:218755254-218756645Esophagus
SE_40583chr2:218752197-218759244Left_Ventricle
SE_42142chr2:218752200-218759229Lung
SE_46178chr2:218753403-218754281Osteoblasts
SE_46178chr2:218754378-218756078Osteoblasts
SE_46622chr2:218754415-218754666Ovary
SE_48107chr2:218752708-218755370Psoas_Muscle
SE_48107chr2:218755390-218756328Psoas_Muscle
SE_48552chr2:218752206-218756933Right_Atrium
SE_49441chr2:218754400-218755161Right_Ventricle
SE_53299chr2:218752197-218754447Spleen
SE_53299chr2:218754461-218755997Spleen
SE_54481chr2:218753378-218811875Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2218753522218753687
Number: 2             
IDChromosomeStartEnd
GH02I217887chr2218752378218754217
GH02I217889chr2218754358218755968
Enhancer Sequence
CCCTTTCCCT TGACCCTCTC TCTTCTCTTG TCTGTCACCA TGTGAGATTT GCCTTTCACC 60
TTCCGCCATG ATTGTGAGAC CTCCCCAGCC ACGTGGAACT GTGAGTCCAT TAAACCTCTT 120
TCTTTTGTAA ATTGCCCAGT CTTGGGTATG TCTTTATCAG CAGCATGAAA ATGGACTAAT 180
ACACCAGGGA ATCCCTAAAT AATCCTATTC CTGAGAGGTG ACACTGATCC CTGGTCTTCA 240
GGCCTTCACT ACTCAGACTC AGAGATGTTA CTCTCTACCC ATTCTCTCCA AGCCACACTG 300
TGCCATTGGA ACAGCATGCT TCTCTCTTAG TATCCTTATC CTTCAAGGTC AAAGGCCACA 360
CCGTGATTAC AGTCAGCAGA CACACATGGC AAGCCAGAGG CTGACAAGGC AGTGCTTGAC 420
CAATCATTCT TTCTTCCCTG AGAAGACTCT CGTTGATCCA CAGCTGCTGT CTCCAGGGCC 480
CTAACCAGAA TTTTCTGCAC ATAAAGACAT CCCATTTCTG GTTGCTGACT CTGAGGCTGG 540
CTATCAACTG TTTTGTGCAA CTATAAGGTG CTGGGTTACC TGAGGACTCA CTCACTTCTT 600
GGGCTTCCAA TTACAATGGC GGGAATAGCC CCCAGCTGGG ACAGCACAGT TCTAGCCAGC 660
CAAGCAAGGT GGGATGATGG GGCACGTGTT GGGACCCTCA GCATGATGAG GCTGGAGAGC 720
TCCAGGACTC ACAGCTCCAG GCCCTTGTTG GCCCAGTCAG TGTGCTCAGG GGCTAAAAAG 780
GCAAATAGGA TGCTTTGGCC TCCAGGCCCT TGTAGTCAGT GCTATTCCCT CATTCTGGAT 840
CCTTTATCCC GTGCGTTCAC TTGGAGGCTT CCTTCTCCCC ACCCAGATCT CATGTTACAC 900
GTCACCTTCT CAGAAGGCCC TTCCATTTGA ATCAGCCCTC TTTCCAGCCC CATCACTCTC 960
TAGCCATCAT AGTTTGCCTT TTCTTTGCAG CTCTCATGAC TATCTGAATT GTTTCCTTAT 1020
ATGTGTAACA TCCACTAGAA GCTGAGCTCC ATAAGCCCTT GCCTGGCGGA TTCAGCACCA 1080
TGTCACCAGT GTGCAGAATG GTGCTGACAT CACGGCAGGT GGCAGGCCCA CAACTCCCAG 1140
CAGCAAACAG AGCTGGGCCT GCGTCCCACC ATCCAGGTCT CCAGTTTGGG CTTGGGTTTC 1200
CCACCATCCT GGCTGCAGCC TCCCCCAAAG ACCTCCTGCC CCTGATGCTG CCTGTGCCTT 1260
CCTGTGCATG AGATGTCTTT GAGCAACATG TCACCCACGG AGCAGGATCC CTCAGGACAG 1320
TGGGTCACAC AACCAGGAGG CACTGCCCTA GCCCAGGCAT TACTAGGCCT TCACGTACTT 1380
TCCAGTTCTG CCACTACTCA CTATAGACCA TGGCCACGCC CCCTCCCTCG GCTCAGCTTC 1440
TAATCTGCAA AATGGGATGC CTAGATCATC ACACGATAGC TCACCGTGAT TCCAGTTTAG 1500
GCTCAAATTC ACCCCCTCTA AGAGGTATTC CCTGACCATC CCTATTAAAA GAGCCCCGTT 1560
CCCCTATCAG TTCTCGTGTC TGCAGTGCCC TCTTTCCTTC CTAGCCTCAT TGCTGTCTGA 1620
CACTGTCTTG TTTGTATGGT TATTTGTTTC ATGTCCATCT CTCTCATTAG GTATCAGCTC 1680
ACCAAGGGAA AGGACTTTTT CCTGTTCACC CAGATATCTC AGTGCTTGGA GCCATAGTAG 1740
ATGATTTAAA TTTTGCTGAA TGAATAAATC CATCCCTGCC CTGTTTCCTG CCTGGGCTAT 1800
TGTGAGACTC CAATGAGACC ATGTGGTTGA AAGCTCTCAG TAAAACTGTC TAAACTCTCC 1860
CAACAGAAGG TGACCCTTAT CATGAGTGTC TGACCTCCCA CAGCAGGGGG CAGTGATGCA 1920
GTCTCCCGTA GACTCATCCA AGCACTGAAG CAATCCTGCT TCCAGGGCCA AGAACAGCAC 1980
ATGCCTTCCT AGACCAGCGC CTTCTTATCC CCAGACTCAT GCTTCCCCAT GAAGGTTGCA 2040
CTGCTCTCTA GCACAGGCCT CAGAGTCAAG TGCTGTGCCA ATCTGCGGGC ACACACCACA 2100
GGCTGGCTCC CGGGCTCTCC TGTGTGCCTG AGCTCACACC ACTGCAGGCT GGCATCTGAA 2160
AACTTGCGCC TGGTACACCC CCACCTAGGC ACAGCTATCC CATCCCTGTG AGTACACAAG 2220
TCTAGTCCCC ACATAGAGTG AGTGCACACA TACATGCAAG GGGCTGTGAG CCCCAGAGAC 2280