EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS188-08756 
Organism
Homo sapiens 
Tissue/cell
Th2 
Coordinate
chr22:50337420-50340710 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GCM1MA0646.1chr22:50338288-50338299CATGCGGGTAC+6.62
PLAG1MA0163.1chr22:50340609-50340623GAGGCCCAAAGGGG+6.37
ZfxMA0146.2chr22:50338091-50338105CAGGCCTCAGCCCC-6.21
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_10057chr22:50337764-50339995CD14
SE_10530chr22:50338223-50338749CD19_Primary
SE_10530chr22:50338855-50340155CD19_Primary
SE_11301chr22:50337371-50340370CD20
SE_12420chr22:50338129-50340096CD3
SE_17545chr22:50337358-50341301CD4p_CD25-_CD45RAp_Naive
SE_17909chr22:50337253-50340777CD4p_CD25-_CD45ROp_Memory
SE_23129chr22:50337861-50338538Colon_Crypt_1
SE_23129chr22:50339336-50339949Colon_Crypt_1
SE_23129chr22:50340142-50347336Colon_Crypt_1
SE_23738chr22:50337894-50338535Colon_Crypt_2
SE_23738chr22:50339474-50339920Colon_Crypt_2
SE_23738chr22:50340192-50347293Colon_Crypt_2
SE_24687chr22:50337135-50338557Colon_Crypt_3
SE_24687chr22:50339454-50339903Colon_Crypt_3
SE_24687chr22:50340156-50348528Colon_Crypt_3
SE_28169chr22:50340100-50347261Fetal_Intestine
SE_29459chr22:50340194-50347426Fetal_Intestine_Large
SE_31381chr22:50336439-50338682Gastric
SE_31381chr22:50338853-50339966Gastric
SE_31381chr22:50340030-50364844Gastric
SE_34375chr22:50337498-50340123HCT-116
SE_35007chr22:50337640-50340278HeLa
SE_41617chr22:50339456-50339853LNCaP
SE_42159chr22:50337434-50338605Lung
SE_42159chr22:50339996-50364887Lung
SE_47471chr22:50339107-50339443Pancreas
SE_47471chr22:50339517-50339940Pancreas
SE_47471chr22:50340157-50349301Pancreas
SE_50117chr22:50337730-50338610Sigmoid_Colon
SE_50117chr22:50339205-50347666Sigmoid_Colon
SE_52469chr22:50337748-50338591Small_Intestine
SE_52469chr22:50338933-50339975Small_Intestine
SE_53398chr22:50337357-50338476Spleen
SE_53398chr22:50338967-50339914Spleen
SE_56937chr22:50340142-50346911VACO_400
SE_61206chr22:50315437-50364432HBL1
SE_61985chr22:50315627-50364432Toledo
SE_62450chr22:50318672-50364388Tonsil
SE_65335chr22:50340176-50344048Pancreatic_islets
SE_68380chr22:50327316-50364640TC32
SE_68381chr22:50327316-50364640TC32
SE_68382chr22:50327316-50364640TC32
SE_69071chr22:50340249-50341775H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr225033847350339938
chr225033898650339884
chr225033880550338926
chr225033802650338636
Number: 1             
IDChromosomeStartEnd
GH22I049942chr225033615950349619
Enhancer Sequence
CCCCCCCACC CCGCCGCCCA GGCCTTTAGG GAAGAACCCA CCCACCAGGC ATGTCAGGAA 60
GGTCGGGTTT TCTCCACGGA TAAGGATCCC CACCTTCGGG GTCATCGGAG GTCACGCTAC 120
CCAGAAGGAA GAAGGTGAAC GCAGGCCGTA GGGCTTCCTG GAGGAGGGGA CCCCGGGGAG 180
CAGCACCCAG CCAGCCAGAC GCACGGGGGT GGCATGTGTG CATAGGCGTG TGAGTGCTGG 240
CATGCATTTA GCGCCAGGGA GGGAGGCCCA GACTCACAGT CTTGCCAAGC TAGACACCTT 300
TAGCCCTGGG CCCCCAAGAG GGGCAGCAAC CCGGCGGGCA GGCTCCTGGC AGTCTGAGGA 360
ACAAGGCCCG GCTGGTAGGG ATGGACATTT CCACTTCAAG ACCCGCCAGA ATCCCCCACC 420
TGCGGGTCAC CCAGGCCATG GCTGGCCACA AGCCGCCCTG CCGGAACTGC ATGTTCTCAG 480
TGTGGGCCCG AAAGGGATGG GGAGGCTCCT GCTCATCCTC AGCTGCACTC CCGCCCCCAC 540
TGCCCCTCTG GGAAGCCCCT GGCGTCTAAC GTCCCATCAG CCAAAGACTT GCCAAGCACA 600
GGCCCAGGCC TGGTCACCCC CAGCAGGGTC ACCTCACTCT GGCCATGGAG GAGGTTGTGA 660
CACAGGATGG CCAGGCCTCA GCCCCACAGA GCTGCCTCCC TGAACCCTGT CCTGGCCTGG 720
GAAGACTGGC TCTCACACTG CTGGGCCTGG GGACCAAGCC TGTGGGCAGA AGCGGCCCTC 780
CAACGCTCAG GACAGGCCTG GGGTTGTCCA GGCCTCCCGG GTCCTGCCTC CTCCTGGACC 840
TGGCCTTGGT CTGAGCACCT GTTCTCTCCA TGCGGGTACC TGGGCCTCTG AAATCCCCGC 900
TGGTGGAGGA GGTGTTGGGT GGCCCAGGAT CACCAGCACA CCAGGTGGCA GCCTCCACCC 960
CAGACCTCAG GCTGCAGTGC CAGGCACCCA GAGCGCCAGG AGCCCACCGC AGTCACAGTG 1020
ACAGCCGGGC CGTGCATCTT GGGGTGCGCT TGCGCCAGCC CAGAGCTCCT GACCGCATGA 1080
TGTCCTGGGG GGTTGGGACC CGGAAAAAAG TCTCACTGCT CACCAGCCCC CCAGGAAACT 1140
CCGCCCCTTT ACAGTGTCGC TGCTCACCAG TACCCCCAGG AAACTCTACG CCCCTTTACA 1200
GTGTCACTGC TCACCAGGTC CCCCAGGAAA CTCTACGCCC CTTTACAGTG TCACTGCTCA 1260
CCAGGTCCCC CAGGAAACTC TACGCCCCTT TACAGTGTCA ACTGCTCACC AGGTCCCCCA 1320
GGAAACTCTA CGCCCCTTTA CAGTGTCACT GCTCACCAGG TCCCCCAGGA AACTCTACGC 1380
CCCTTTACAG TGTCACTGCT CACCAGGTCC CCCAGGAAAC TCTACGACCC TTTACAGTGT 1440
CACTGATCAC CAGGTCCCCC AGGAAACTCC GCCCCTTTAC AGTGTCACTG CTCACCAGCC 1500
CCCCAGGAAA CTCCGCCCCT TTACAGTGTC ACTGCTCACC AGCCCCCCAG GAAACTCCGC 1560
CCCTTTACAG TGTCACTGCT CACCAGCCCC CCAGGAAACT CTGCCCCTTT ACAGTGTCAC 1620
TGCTCACCAG TCCCCCCAGG AAACTCTGCC CCTTTACAGT GTCACTGCTC ACCAGGTCCC 1680
CCAGGAAACT CCGCCCCTTT ACAGTGTCGC TGCTCACCAG CCCCCCCCAG GAAACTCCGC 1740
CCCTTTACAG TATTGCTGCT CACCAGCCCC CCAGGAAACT CCGCCCCTTT ACAGTGTCGC 1800
TGCTCACCAG CCCCCCCAGG AAACTCCGCC CCTTTACAGT GTTGCTGCTC ACCAGTCCCC 1860
CCCAGGAAAC TCCGCCCCTT TACAGTGTCG CTGCTCACCA GCCCCCCAGG AAACTCCGCC 1920
CCTTTACAGT GTCACTGCTC ACCAGCCCCC CAGGAAACTC CGCCCCTTTT GGGGCCAGAG 1980
ATGCTGTGAG AAGTGGCCTT TTATTATATA AAACTGTTTT ATGCAGAATT TAAGATGTAC 2040
ATGTGACCCC TGAGATTAAA CCACAGCCCC AAACAGCTCC CTGATTTTAG CCTTGTAGGA 2100
GACCCTGGGG CAGAGGGAAA CTGCTAAACC AGACTTGGAT TCCAGACCCA CCTGGAAGTC 2160
ATAAATGTGT GTTGTTTTAA GCCACTATAA TTTGGAGTCG TTTGTGACAC AGCAGAGCAA 2220
CAGATTACCA TCATGGTGTT GAAGGTAGAG CCAGCTGGGC TTGCTGGCTG ACTCCAGGGC 2280
ATTGGAGGAC GCCAGAGCAT TGACCTGAGC CCCTGGCAGG TGTGGCTGGC AGCATTGGGA 2340
CAAGGACAAC GAAGGCTGCA AGTCAAGAAC TCTGCGCTGG GGCCAGGCGG CGGCTCACAC 2400
CTGCAATCCC AGCACTGTGG GAGGCTGAGC CTGATGGATC ACCTGAGGTC AGGTTTGAGT 2460
TCAGCCTGCC CAACATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT TAGCCAGGCA 2520
TTGTGGTGCA TTCCTGTAAT CCCAGCTACT CAGGAGGCTG AGGCAGGAGA ATCACTTGAA 2580
CCCGGGAGGT GGAGGTTGCA GTGAGCTGAG ATCACACCAC TGCACTCCAG CCTGGGCAAA 2640
AGAGTGAGAC TCCATCACAA AAAAAAAAAG ACTTTGGATA AATATGTGTT GTCCAACAAC 2700
TTTGGATAAC AGAAAACACC ACAACAAGTT GAGAAATGGA TTACAGAAAA AAGAACGAGC 2760
TTCGTACGTT AGCACCTATA ATATCATTTC ATCCTGCATT TTGAACAATG AACCCTGAAT 2820
TCTCATGTGC GCTGGGCTCT GCAAATCATG TGGCTGCTCC CCATAGTCAG GAAGGAGAGT 2880
GGGACTCAGG GGAGGAGGCA GGATGAGCTG AGACCCAGGC TGCCTGTCCC TACCACTGAC 2940
CAGGACAGCG TTCCAGCCTC CCCGTCTGCT CAGAATCTGC CCTGACCTGC TCCACACCCC 3000
CGCAGGCCCG CAGGGGAGGG CAGAACTAGA AGGGACCAGC GCATAGGGAC CTGGGGGTGC 3060
TGGCACTGAG GTCTCTGGGC CTGGGATGCT GACCTTCCCG GAGCCCTGAG CTGGGCCAGG 3120
ACGAGGTCTT CCCATCAGAC TTGCCGCTGG CTAGGTGACC GGCCTGTCTC ACAGATGAAA 3180
ATATATTCTG AGGCCCAAAG GGGGCCCAGA CCCTGACTTT GTGGCCCAGA GCCAGGTTCT 3240
CCCCATAACC AGCAGGCTTC TTTACCCACA GGCCACTGTC CACCCAAGCC 3290