EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS093-20892 
Organism
Homo sapiens 
Tissue/cell
HL-60 
Coordinate
chr22:42695560-42697700 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6002676chr2242697216hg19
TF binding sites/motifs
Number: 25             
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
ZNF263MA0528.1chr22:42697672-42697693GGAGCAGCAAGGGAGGGAAGG+6.82
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
TGGAGGGGAA TCACATGTCC CACTGGTCAC CAGTCCCTCT TGCCTTTCTG TCCCAGCTAG 60
CAGCTCTCCA ACCTCTGTAC CTCTCCCCGA ACGCAGGCCC CCCTGCCCGC ACCCCAACAC 120
TTCAAGACCT CCTAGGAGTG ACCTGGCTGG GGTCTCTCTA GGTCAGGTAA TTAATAGCAG 180
GAGGGAAGTG CAATTAGCAG GTACCTGGAG TGGGGTCGGT AAGAGAGAAT AGCAGAGGAG 240
GAGGAAGTGG TGGGGATGGG GGAGGGGAAG AGAGAAGGGG GAGAAGGAAG CGGAGGGGAG 300
GAGGGAGGAG GGAAAAGACA GAAAGGGGTA GAAGGGAAGC TTGGAGCGGG TGGAGGAGGA 360
GGGGGAAAGG GAGCAGAGGA AGAAAGGAGA GGAGGGGAAG GAAGGGCGGG GAGGGGGAGG 420
GGGAGGGGCG CGCTGAAATC ACCCGCAACA TCAAAGCCTT CCCCAGCCGC AAAGCAGTCA 480
CGTGCAGCCT GGTTCCTTTC GTTCCTTCGT TCCTTCGCTG GTAGAAGCCG CTGGGCCTGG 540
GGCTGCTGAA GGAATTTTAA AACGAGGCAG ATTGTCTGGA ATATCAGGGG GTTAGGGGAA 600
TGCGGTTTTA TCTCAAGGCA GGGTAAGGGG AGGCAGGTTT TGAAACCTGT TCCCCCAAGG 660
AGAGCGGCAG GGCTTTGGGG CCTCTGCTAG GAGGCTGGGC AGGTGGCCAA GAGTGAAGAC 720
CACCCAGCTA CTCCTGCCGG TGAGAGCTCG TGGCTGGGCC AGCCCAGATA TCAACAGAAG 780
CCAGAAATCT AGATTTGTAT GTGAAAACTT CCCTGTTTTA ATTTTGGCTC AAACTAAAAA 840
AAAAAAGAAA AAAAGCGCCA CATGGGCCAA ATAGAGCATG TCCTGACTGG GGCCCAGAAC 900
CTCGGTCACC TCCCACTTCT GATGGTGGGC AGCAACGCTT TTGTTTCCCA GGGGGCACTG 960
AGGCCCAGGA AGGGAAAGGC ACTTGTTCAG GGACACACAC AGTGAGTGCT CAAGGGGTGC 1020
GGGCTAAGAC TTGGGGTCTC AGGACTCCCA TGCCTGAAGC CTCCTGCGGT CAGCAGCCCA 1080
AGGGGCAGGG CTGTGGCTGC TGGGAAAGGG AAGTATAGGG AGGTTAGTGG CAGGGGAGGG 1140
TCTCAGAAAA CCCCTCGTCC AGCCCAGGGC CAACACACTC AGCCCCACTC ATCACCCTGA 1200
TGACTAACCC AGGCCTGCCT CTCTGCCTTT GCCTCTGCTC AGCCCATCCT CCCTATCCAC 1260
TCCTGACATT CCCTCCTCCC CCTGCCAAGA CCTGGGCAGC TTCCCCTCCC CCGAGCCCCA 1320
CCTGCAGAAT GCACCATGCA TTCAACCATT CATTCTTCTG TTGCTCCCCA AGGCCCTGAG 1380
TCAGCCTTAA CCCCACCTTC AGAGGCCAGG ACAGGGGAGG GTGTTTAGGA TAGAGAGGTG 1440
TGGCCTCCAA GGAGGAAGCA GCTACCTCTG TAGGGTGGCG GTAGGGGAGT CTCCCCAAAG 1500
GAAGGTCCTA GGGCAGAGCA TGGCATCTGC ACTTACCAGG GTGGAGGTGT AAATGGCTGC 1560
TGGAAGCCAG AGGCAAGGCT GGGAGGAGGT GGATGTGGGG GTTCAGAAAT GCGGAAGTTT 1620
ATCTTGCGGG CACTAGGGAG CCGTTGGAGG TGTGTAAGCA GGAGAGAGGT CGGCTCAGAT 1680
CTTCACTATG GGGCTGTCAG GACAAGGCGA GGATGGAGTC ATTCATAGGT TCAACAAGTG 1740
TTTGCTGAGC ACTTACTCTG TGCCACGCCC CAGGGAGACA GAGGAGAGCC AGACAGACAA 1800
GGCGTGCACC TTGGGGAGAC AGACGTGACC ACACAACCAC CACCACAGGG TGAGGGGGCT 1860
ATGGTGGGGG CTGGACTGGG TAAGGCACGT GGCCTGGTCC CTCCAAAGAG GAATCCACCT 1920
GCAAGGTGAG GACAGGAGGG GACACTGTTC CCAGCCAAGG AGGTGGCATG CACACAGGCC 1980
CAGAGGTGGA GAAAGCAGGG CTTCCTAAGT CAAAGTGATT CGACAGGCGG AGGTGTCTGC 2040
AAGAGCCATG CCAAAGGTGA CAGAGCTCCC TGGCGTAGCT CCAGGGCAAT GGAAACCTTT 2100
GGGAGGGGTC TGGGAGCAGC AAGGGAGGGA AGGTGGGAAG 2140