EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-16468 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr22:42695300-42697670 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6002676chr2242697216hg19
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr22:42696059-42696077CGTTCCTTCGTTCCTTCG-6.54
EWSR1-FLI1MA0149.1chr22:42696055-42696073CTTTCGTTCCTTCGTTCC-6.95
MYCMA0147.3chr22:42697442-42697454AGGCACGTGGCC-6.07
SPI1MA0080.4chr22:42697165-42697179GAAATGCGGAAGTT+6.68
SPIBMA0081.2chr22:42697167-42697179AATGCGGAAGTT+6.27
ZNF263MA0528.1chr22:42695935-42695956GAGGAAGAAAGGAGAGGAGGG+6.03
ZNF263MA0528.1chr22:42695830-42695851AGAGAAGGGGGAGAAGGAAGC+6.08
ZNF263MA0528.1chr22:42695944-42695965AGGAGAGGAGGGGAAGGAAGG+6.1
ZNF263MA0528.1chr22:42695810-42695831TGGGGATGGGGGAGGGGAAGA+6.23
ZNF263MA0528.1chr22:42695953-42695974GGGGAAGGAAGGGCGGGGAGG+6.26
ZNF263MA0528.1chr22:42695956-42695977GAAGGAAGGGCGGGGAGGGGG+6.33
ZNF263MA0528.1chr22:42695938-42695959GAAGAAAGGAGAGGAGGGGAA+6.36
ZNF263MA0528.1chr22:42695947-42695968AGAGGAGGGGAAGGAAGGGCG+6.4
ZNF263MA0528.1chr22:42695796-42695817GGAGGAGGAAGTGGTGGGGAT+6.58
ZNF263MA0528.1chr22:42695839-42695860GGAGAAGGAAGCGGAGGGGAG+6.69
ZNF263MA0528.1chr22:42695836-42695857GGGGGAGAAGGAAGCGGAGGG+6.79
ZNF263MA0528.1chr22:42695853-42695874AGGGGAGGAGGGAGGAGGGAA+6.84
ZNF263MA0528.1chr22:42695793-42695814AGAGGAGGAGGAAGTGGTGGG+6.93
ZNF263MA0528.1chr22:42695966-42695987CGGGGAGGGGGAGGGGGAGGG+7.01
ZNF263MA0528.1chr22:42695817-42695838GGGGGAGGGGAAGAGAGAAGG+7.11
ZNF263MA0528.1chr22:42695914-42695935GGAGGAGGGGGAAAGGGAGCA+7.5
ZNF263MA0528.1chr22:42695856-42695877GGAGGAGGGAGGAGGGAAAAG+7.69
ZNF263MA0528.1chr22:42695908-42695929GGTGGAGGAGGAGGGGGAAAG+8.08
ZNF263MA0528.1chr22:42695911-42695932GGAGGAGGAGGGGGAAAGGGA+9.32
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_23330chr22:42695863-42698813Colon_Crypt_1
SE_23842chr22:42695766-42696384Colon_Crypt_2
SE_23842chr22:42696407-42698797Colon_Crypt_2
SE_25072chr22:42694701-42695817Colon_Crypt_3
SE_25072chr22:42695921-42698957Colon_Crypt_3
SE_50938chr22:42695852-42698100Sigmoid_Colon
SE_56829chr22:42695891-42696837VACO_400
SE_56829chr22:42697117-42697976VACO_400
SE_65474chr22:42695910-42696986Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr224269580042697556
chr224269600542696062
Number: 1             
IDChromosomeStartEnd
GH22I042298chr224269488042697851
Enhancer Sequence
GGAACTGAGG GTCCTTCCCA GCCCCTCTCC CCACATCCAG CCCCCTGCTC TGGCACTCTC 60
TCCATCTGCC TCTCACACAG TCCTTACCTT GCTCTCCCTC CCCATGGACT CTCTCTCCCA 120
TCTCCCCTCC CCACTCCTAG CCAACCTCCA ATGCCCTGGG GCCTCAATTT CCCCCAGGAC 180
AAAGGGGCCT CAAGGCCTCA TGAACAGAAC ATGCTGGCAG TGGTGGGTCA CCCAGGAACC 240
CCGAGGAACT GGAATGGGGG TGGAGGGGAA TCACATGTCC CACTGGTCAC CAGTCCCTCT 300
TGCCTTTCTG TCCCAGCTAG CAGCTCTCCA ACCTCTGTAC CTCTCCCCGA ACGCAGGCCC 360
CCCTGCCCGC ACCCCAACAC TTCAAGACCT CCTAGGAGTG ACCTGGCTGG GGTCTCTCTA 420
GGTCAGGTAA TTAATAGCAG GAGGGAAGTG CAATTAGCAG GTACCTGGAG TGGGGTCGGT 480
AAGAGAGAAT AGCAGAGGAG GAGGAAGTGG TGGGGATGGG GGAGGGGAAG AGAGAAGGGG 540
GAGAAGGAAG CGGAGGGGAG GAGGGAGGAG GGAAAAGACA GAAAGGGGTA GAAGGGAAGC 600
TTGGAGCGGG TGGAGGAGGA GGGGGAAAGG GAGCAGAGGA AGAAAGGAGA GGAGGGGAAG 660
GAAGGGCGGG GAGGGGGAGG GGGAGGGGCG CGCTGAAATC ACCCGCAACA TCAAAGCCTT 720
CCCCAGCCGC AAAGCAGTCA CGTGCAGCCT GGTTCCTTTC GTTCCTTCGT TCCTTCGCTG 780
GTAGAAGCCG CTGGGCCTGG GGCTGCTGAA GGAATTTTAA AACGAGGCAG ATTGTCTGGA 840
ATATCAGGGG GTTAGGGGAA TGCGGTTTTA TCTCAAGGCA GGGTAAGGGG AGGCAGGTTT 900
TGAAACCTGT TCCCCCAAGG AGAGCGGCAG GGCTTTGGGG CCTCTGCTAG GAGGCTGGGC 960
AGGTGGCCAA GAGTGAAGAC CACCCAGCTA CTCCTGCCGG TGAGAGCTCG TGGCTGGGCC 1020
AGCCCAGATA TCAACAGAAG CCAGAAATCT AGATTTGTAT GTGAAAACTT CCCTGTTTTA 1080
ATTTTGGCTC AAACTAAAAA AAAAAAGAAA AAAAGCGCCA CATGGGCCAA ATAGAGCATG 1140
TCCTGACTGG GGCCCAGAAC CTCGGTCACC TCCCACTTCT GATGGTGGGC AGCAACGCTT 1200
TTGTTTCCCA GGGGGCACTG AGGCCCAGGA AGGGAAAGGC ACTTGTTCAG GGACACACAC 1260
AGTGAGTGCT CAAGGGGTGC GGGCTAAGAC TTGGGGTCTC AGGACTCCCA TGCCTGAAGC 1320
CTCCTGCGGT CAGCAGCCCA AGGGGCAGGG CTGTGGCTGC TGGGAAAGGG AAGTATAGGG 1380
AGGTTAGTGG CAGGGGAGGG TCTCAGAAAA CCCCTCGTCC AGCCCAGGGC CAACACACTC 1440
AGCCCCACTC ATCACCCTGA TGACTAACCC AGGCCTGCCT CTCTGCCTTT GCCTCTGCTC 1500
AGCCCATCCT CCCTATCCAC TCCTGACATT CCCTCCTCCC CCTGCCAAGA CCTGGGCAGC 1560
TTCCCCTCCC CCGAGCCCCA CCTGCAGAAT GCACCATGCA TTCAACCATT CATTCTTCTG 1620
TTGCTCCCCA AGGCCCTGAG TCAGCCTTAA CCCCACCTTC AGAGGCCAGG ACAGGGGAGG 1680
GTGTTTAGGA TAGAGAGGTG TGGCCTCCAA GGAGGAAGCA GCTACCTCTG TAGGGTGGCG 1740
GTAGGGGAGT CTCCCCAAAG GAAGGTCCTA GGGCAGAGCA TGGCATCTGC ACTTACCAGG 1800
GTGGAGGTGT AAATGGCTGC TGGAAGCCAG AGGCAAGGCT GGGAGGAGGT GGATGTGGGG 1860
GTTCAGAAAT GCGGAAGTTT ATCTTGCGGG CACTAGGGAG CCGTTGGAGG TGTGTAAGCA 1920
GGAGAGAGGT CGGCTCAGAT CTTCACTATG GGGCTGTCAG GACAAGGCGA GGATGGAGTC 1980
ATTCATAGGT TCAACAAGTG TTTGCTGAGC ACTTACTCTG TGCCACGCCC CAGGGAGACA 2040
GAGGAGAGCC AGACAGACAA GGCGTGCACC TTGGGGAGAC AGACGTGACC ACACAACCAC 2100
CACCACAGGG TGAGGGGGCT ATGGTGGGGG CTGGACTGGG TAAGGCACGT GGCCTGGTCC 2160
CTCCAAAGAG GAATCCACCT GCAAGGTGAG GACAGGAGGG GACACTGTTC CCAGCCAAGG 2220
AGGTGGCATG CACACAGGCC CAGAGGTGGA GAAAGCAGGG CTTCCTAAGT CAAAGTGATT 2280
CGACAGGCGG AGGTGTCTGC AAGAGCCATG CCAAAGGTGA CAGAGCTCCC TGGCGTAGCT 2340
CCAGGGCAAT GGAAACCTTT GGGAGGGGTC 2370