EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS041-02599 
Organism
Homo sapiens 
Tissue/cell
EWS502 
Coordinate
chr1:223920410-223923250 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs140084787chr1223920445hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr1:223922394-223922411TGGCACACCATGTACCA-6.01
Gata4MA0482.1chr1:223920574-223920585TCTTATCTCCC+6.62
Nr2f6(var.2)MA0728.1chr1:223923013-223923028GAGGTCAGGAGTTCA+6.22
Nr5a2MA0505.1chr1:223921780-223921795GACCTCAAGGCCAGC+6.22
USF2MA0526.2chr1:223921349-223921365CCAGGTCACGTGAGTC+6.03
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00224chr1:223917623-223923297Adipose_Nuclei
SE_01908chr1:223920427-223922082Aorta
SE_02306chr1:223920308-223921944Astrocytes
SE_04026chr1:223920429-223923012Brain_Anterior_Caudate
SE_05036chr1:223920530-223922321Brain_Cingulate_Gyrus
SE_05972chr1:223920132-223922577Brain_Hippocampus_Middle
SE_07159chr1:223920244-223923166Brain_Hippocampus_Middle_150
SE_07996chr1:223920284-223922259Brain_Inferior_Temporal_Lobe
SE_09681chr1:223920277-223921825CD14
SE_19702chr1:223921073-223922029CD4p_CD25-_Il17p_PMAstim_Th17
SE_23408chr1:223920555-223922971Colon_Crypt_1
SE_24051chr1:223920713-223921438Colon_Crypt_2
SE_24051chr1:223921499-223922031Colon_Crypt_2
SE_24051chr1:223922112-223922463Colon_Crypt_2
SE_25230chr1:223920636-223922879Colon_Crypt_3
SE_26209chr1:223920732-223921934Duodenum_Smooth_Muscle
SE_26925chr1:223921184-223922005Esophagus
SE_31491chr1:223920239-223923646Gastric
SE_33950chr1:223920559-223921591HCC1954
SE_38254chr1:223917692-223922239HUVEC
SE_41495chr1:223920316-223922995Left_Ventricle
SE_42269chr1:223920225-223923100Lung
SE_45872chr1:223920277-223921720Osteoblasts
SE_49408chr1:223920327-223922010Right_Atrium
SE_50365chr1:223920440-223922961Sigmoid_Colon
SE_53249chr1:223920551-223922027Small_Intestine
SE_65644chr1:223920306-223922506Pancreatic_islets
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1223921475223921876
chr1223922041223922091
chr1223922066223922385
Number: 2             
IDChromosomeStartEnd
GH01I223735chr1223923230223924466
GH01I223730chr1223917704223922480
Enhancer Sequence
GCTCTTATTC AAGATGGAGT TGCTCTAGTT CACACGCCTC TGACACATGT TCAGAAATAA 60
TGGTGATTTT CTTCTACAGG TGGGGACGTT AGCATTATAA TGACATGGTA AAGTTCTGAA 120
GGTAACAAGG GGTTGCCTGT TCCAGTTTCT GCCAGTTTTG GGGGTCTTAT CTCCCTCTGG 180
TATCTGGGCA GAGGTCAAGA AGCTCTGGCA CCATCAGGGG CCAGCTTGTT TCTTTAAGCA 240
GCTGTGCCTA CAAATAAAGG GACTAAAGAA AACAATAAGA AAACCCAGTT ATTTCCTGGG 300
GGTTGCTCTG GTATCCAGCG TGTTTTACTT CACCAAGCGC AATTCTTCCC AGTGCAGGCA 360
CTGGGTGTAA CTGTGACAGC CAGCACCAAC CTGCCCACAC ACCTCCTGTC CTGCAGGACT 420
GTCAGCAGCC TCTGCACTAT AGTGTGACAG AGCCACAGGT AGCTCAGGTG TGCCTCAGCC 480
CAGCCTCTCC TGCACTCCCC CTCCCCTGGC TCCCCAACTC TGCCTCACTT CTGTTTGTGA 540
AGGAAAGACA GCAGTAGCGG AAGGGAAAGA AGGAGAAAAT GCAGAGCAAA TATTATGCTT 600
TCCTCTTGGA AAACCTCCAG GAGCTGCAAA TATTAGTAAT CCAGCTGCAT CCCACCCCCC 660
AGGATGGGCT GGGCCTGTCA CACAGCCAAC CTTCAGGATG CAGACACCCA GGCTGGGGAG 720
CACAGCTCTG GAAATTTACT GACATGGCCC TGAATGAATT TATCTTTTCA GTAGAAGGCC 780
CTGGAGTTTA AAGGAGTCAT TCATAAGGTC TGTCTGGGAG TGCCTTGTCC TCAGAGGAGG 840
GTCTGGGTGG GTTGGAGTGG AAGGAAGGGC TGGCTACCTG GTGTGCTCTC CGTGGGTCCC 900
CAAGAAAGGC AGCCCTGCTG GGGGCAGTGA AGCCCTTATC CAGGTCACGT GAGTCTTGGA 960
AGGGGAAGGC TGCTGTGCTT AACGATTCAA AAACACAAAT CAAACCTCCT TTCCCAAACA 1020
AATTAGAAGG TGTGGAGGAA GCTTGAATTC AGAGAGGATT TCCCAGAGAC CCATAGGCAA 1080
AAGTGGCTTA ACTGAGCCCA GTGGGTGTCC CAGAATGGGC CAGAGAGAAT GACACTAAAA 1140
AGTCTTTGAA CAAATGAGCA AATGAATACA GGAATGCTCA TCTGCCATAG GCACAAACGT 1200
GGTAAACGTT CCCTGAGAGA ACTGACAGCC CAGGGGTGCA GGGAGAGAAA CGGTCCCAAC 1260
TGCAGACTGG GTCCCAACTG CAGACTCGGT CCCAACTGCA GACTCAGGAG GAGGGAGGCT 1320
GTTAAGGGGC CGTCTTTCCT TCTGTTATGT GAGGAGAAAA GCAGGGAAGG GACCTCAAGG 1380
CCAGCCTCTC CCAGGAGCTG CTGTTCTCAG CCCCGGGATC CAGCGCTACA GGGAAGTGCA 1440
GGGGAGGCTC CACAGTCCCG GCTGGAGACC CGGTCAGGCC TGGGTGGCCA CTCTTCTTTG 1500
TAGTGGCCAC CCTCGTGTCA CCAGCAAATG CTTTTGTATC TACACCCTTC TCAGTGCTCC 1560
CCCTCTTTTA AAAAATGTAC TTTCTTTTTT TAAAAAGAGT TGGGTCTTGC CTTGTCACCT 1620
ATGCTGGAGT GCAGTGTTGC TGTCACAGCT CACTGCAAAC TCCACCTCCT GGGCTCAACC 1680
CATCCTCCCA CCTCAGCCTC CCAGGTAGCT GGGACCACAG GCACACACCA GGACACCTCG 1740
CCCAGTGCTC ACTATTTACC TTTATTTCTT CCTTATTCGG ACACCCCTTG CTTCCAAAGA 1800
AGAGTTTCGG AAGGCTCAAG ACGGTGAGAC AGACACCTTA TGCACTGCTT CACTCTCCCC 1860
CGCAGCTCCC CTCCCTCCTC ACTGACCCCC GGCCACAACC CTCTCTCCTT GCCCCTCACC 1920
AGCCGGCACC CTTGGCAACC CTGGCACCCT TTCGAGGACA AGACTGCCAA ATGTGGCCAA 1980
GGTCTGGCAC ACCATGTACC AATCGAAACT CCACTTCCCT TGAGTTTCAG TTTCCACGCC 2040
TATAAAATTA GCAAATGAAA AGAGCAAACA CTTGGAGACA CTGTTCTCAA TGCTTTGCAT 2100
ATTTTTTTCA TTTAATTCTC AGTGCCATGA GACAGTCTAT TATTATTAAA CCTATGTTAT 2160
ATATGAGGAA ACTGAGGCAC AGAGGGAGTA GTTTCCCCAG GTCACAGTCA GGATTTGAAC 2220
TCCATGGTCT GGCTCTAGTG TTTCCCAACC ATTCGGGGTG GGAGTGGGAG AGAAACCAGA 2280
CTGCTCTCCC TAGAAAACAG CATGTGTTTG CATGTGTGCC AAATTTGCAC AAAACATTTG 2340
GGGTTCCAGG TCTCTAAAGC CCATCCATGG AACCCCGGTT TCCCTTCTCT CACGTGATCC 2400
TAACAACCTG CCGAGGATAC ACCTCATCAT GATCCTCCTT TCACAGCTGA GAACACACCA 2460
GCTTAGAGAA ATTAAGAAGT GTATCCAAGC TCACACAATC TTAAGTGGCC AGATCAGGAC 2520
CAAAATCCAG GTCCTCTGGC TGGGCGCAGT GGCTCATGCA TGTAATCCCA GCTCTTTGGG 2580
TGGCCAAGGC GGGTGGATCA CCTGAGGTCA GGAGTTCAAG ACCAGCTTGG CCAACATGGT 2640
GAAACCCCAT CTCTACTAAA AATACAAAAA TTAGCTGGGC ATGGTGGTGG GCGCCTGTAA 2700
TCCCAGCTAC TCAGGAGGCT GAGGCAGGAG AATTGCTTGA ACCCAGGAAG CAGAGGTTGC 2760
AGTGAGCTAA GATGGAGCCA TTGCACTCCA GCCTGGGCAA CAGAGTGAGA CTCTATCTAA 2820
AAAAAAAAAA AAAAAAATTT 2840