EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS050-45245 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr22:42695030-42697800 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6002676chr2242697216hg19
TF binding sites/motifs
Number: 26             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr22:42697687-42697705GGAAGGTGGGAAGCAATG+6.3
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
CAGAGAATAA CCATGGCAGT GATGGGTGGG CTCCAAGGGT TCCCACACCC ACCGCCTGCC 60
CAGACCCCTG CTGTGGAGGG GAACGGAGAC CTGGAGGGGT ACCCCCAAAA ATCTGGACTT 120
GGCCCTGCAG GCTTCTCTGG CCTTTAGAAG GCACGGGAGG ATGGGGGCAA GGGGGCGGTA 180
GGCAGACAGC AAGAGCAACC AGTGAGCCCA GAGGACAATC ACAGGGAGGA CGGCGGCAAG 240
GAGGTGAGGC CATGTCTGGC TGGGGGTGCA GGAACTGAGG GTCCTTCCCA GCCCCTCTCC 300
CCACATCCAG CCCCCTGCTC TGGCACTCTC TCCATCTGCC TCTCACACAG TCCTTACCTT 360
GCTCTCCCTC CCCATGGACT CTCTCTCCCA TCTCCCCTCC CCACTCCTAG CCAACCTCCA 420
ATGCCCTGGG GCCTCAATTT CCCCCAGGAC AAAGGGGCCT CAAGGCCTCA TGAACAGAAC 480
ATGCTGGCAG TGGTGGGTCA CCCAGGAACC CCGAGGAACT GGAATGGGGG TGGAGGGGAA 540
TCACATGTCC CACTGGTCAC CAGTCCCTCT TGCCTTTCTG TCCCAGCTAG CAGCTCTCCA 600
ACCTCTGTAC CTCTCCCCGA ACGCAGGCCC CCCTGCCCGC ACCCCAACAC TTCAAGACCT 660
CCTAGGAGTG ACCTGGCTGG GGTCTCTCTA GGTCAGGTAA TTAATAGCAG GAGGGAAGTG 720
CAATTAGCAG GTACCTGGAG TGGGGTCGGT AAGAGAGAAT AGCAGAGGAG GAGGAAGTGG 780
TGGGGATGGG GGAGGGGAAG AGAGAAGGGG GAGAAGGAAG CGGAGGGGAG GAGGGAGGAG 840
GGAAAAGACA GAAAGGGGTA GAAGGGAAGC TTGGAGCGGG TGGAGGAGGA GGGGGAAAGG 900
GAGCAGAGGA AGAAAGGAGA GGAGGGGAAG GAAGGGCGGG GAGGGGGAGG GGGAGGGGCG 960
CGCTGAAATC ACCCGCAACA TCAAAGCCTT CCCCAGCCGC AAAGCAGTCA CGTGCAGCCT 1020
GGTTCCTTTC GTTCCTTCGT TCCTTCGCTG GTAGAAGCCG CTGGGCCTGG GGCTGCTGAA 1080
GGAATTTTAA AACGAGGCAG ATTGTCTGGA ATATCAGGGG GTTAGGGGAA TGCGGTTTTA 1140
TCTCAAGGCA GGGTAAGGGG AGGCAGGTTT TGAAACCTGT TCCCCCAAGG AGAGCGGCAG 1200
GGCTTTGGGG CCTCTGCTAG GAGGCTGGGC AGGTGGCCAA GAGTGAAGAC CACCCAGCTA 1260
CTCCTGCCGG TGAGAGCTCG TGGCTGGGCC AGCCCAGATA TCAACAGAAG CCAGAAATCT 1320
AGATTTGTAT GTGAAAACTT CCCTGTTTTA ATTTTGGCTC AAACTAAAAA AAAAAAGAAA 1380
AAAAGCGCCA CATGGGCCAA ATAGAGCATG TCCTGACTGG GGCCCAGAAC CTCGGTCACC 1440
TCCCACTTCT GATGGTGGGC AGCAACGCTT TTGTTTCCCA GGGGGCACTG AGGCCCAGGA 1500
AGGGAAAGGC ACTTGTTCAG GGACACACAC AGTGAGTGCT CAAGGGGTGC GGGCTAAGAC 1560
TTGGGGTCTC AGGACTCCCA TGCCTGAAGC CTCCTGCGGT CAGCAGCCCA AGGGGCAGGG 1620
CTGTGGCTGC TGGGAAAGGG AAGTATAGGG AGGTTAGTGG CAGGGGAGGG TCTCAGAAAA 1680
CCCCTCGTCC AGCCCAGGGC CAACACACTC AGCCCCACTC ATCACCCTGA TGACTAACCC 1740
AGGCCTGCCT CTCTGCCTTT GCCTCTGCTC AGCCCATCCT CCCTATCCAC TCCTGACATT 1800
CCCTCCTCCC CCTGCCAAGA CCTGGGCAGC TTCCCCTCCC CCGAGCCCCA CCTGCAGAAT 1860
GCACCATGCA TTCAACCATT CATTCTTCTG TTGCTCCCCA AGGCCCTGAG TCAGCCTTAA 1920
CCCCACCTTC AGAGGCCAGG ACAGGGGAGG GTGTTTAGGA TAGAGAGGTG TGGCCTCCAA 1980
GGAGGAAGCA GCTACCTCTG TAGGGTGGCG GTAGGGGAGT CTCCCCAAAG GAAGGTCCTA 2040
GGGCAGAGCA TGGCATCTGC ACTTACCAGG GTGGAGGTGT AAATGGCTGC TGGAAGCCAG 2100
AGGCAAGGCT GGGAGGAGGT GGATGTGGGG GTTCAGAAAT GCGGAAGTTT ATCTTGCGGG 2160
CACTAGGGAG CCGTTGGAGG TGTGTAAGCA GGAGAGAGGT CGGCTCAGAT CTTCACTATG 2220
GGGCTGTCAG GACAAGGCGA GGATGGAGTC ATTCATAGGT TCAACAAGTG TTTGCTGAGC 2280
ACTTACTCTG TGCCACGCCC CAGGGAGACA GAGGAGAGCC AGACAGACAA GGCGTGCACC 2340
TTGGGGAGAC AGACGTGACC ACACAACCAC CACCACAGGG TGAGGGGGCT ATGGTGGGGG 2400
CTGGACTGGG TAAGGCACGT GGCCTGGTCC CTCCAAAGAG GAATCCACCT GCAAGGTGAG 2460
GACAGGAGGG GACACTGTTC CCAGCCAAGG AGGTGGCATG CACACAGGCC CAGAGGTGGA 2520
GAAAGCAGGG CTTCCTAAGT CAAAGTGATT CGACAGGCGG AGGTGTCTGC AAGAGCCATG 2580
CCAAAGGTGA CAGAGCTCCC TGGCGTAGCT CCAGGGCAAT GGAAACCTTT GGGAGGGGTC 2640
TGGGAGCAGC AAGGGAGGGA AGGTGGGAAG CAATGTTTGC AGGCTGGGGA GACCTGGCTG 2700
CGTCCCTTGG CTCCCTGAAG TCTGTCGTGG GGAACAGGGG ACTCCCTTTC TCACTGCCAG 2760
CGGGCAAAAC 2770