EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS022-09820 
Organism
Homo sapiens 
Tissue/cell
CD4+ 
Coordinate
chr22:50338270-50340900 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GCM1MA0646.1chr22:50338288-50338299CATGCGGGTAC+6.62
PLAG1MA0163.1chr22:50340609-50340623GAGGCCCAAAGGGG+6.37
Number of super-enhancer constituents: 45             
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_34375chr22:50340613-50344021HCT-116
SE_35007chr22:50337640-50340278HeLa
SE_41617chr22:50339456-50339853LNCaP
SE_41617chr22:50340249-50340536LNCaP
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_53398chr22:50338967-50339914Spleen
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: 3             
ChromosomeStartEnd
chr225033847350339938
chr225033898650339884
chr225033880550338926
Number: 1             
IDChromosomeStartEnd
GH22I049942chr225033615950349619
Enhancer Sequence
CTGAGCACCT GTTCTCTCCA TGCGGGTACC TGGGCCTCTG AAATCCCCGC TGGTGGAGGA 60
GGTGTTGGGT GGCCCAGGAT CACCAGCACA CCAGGTGGCA GCCTCCACCC CAGACCTCAG 120
GCTGCAGTGC CAGGCACCCA GAGCGCCAGG AGCCCACCGC AGTCACAGTG ACAGCCGGGC 180
CGTGCATCTT GGGGTGCGCT TGCGCCAGCC CAGAGCTCCT GACCGCATGA TGTCCTGGGG 240
GGTTGGGACC CGGAAAAAAG TCTCACTGCT CACCAGCCCC CCAGGAAACT CCGCCCCTTT 300
ACAGTGTCGC TGCTCACCAG TACCCCCAGG AAACTCTACG CCCCTTTACA GTGTCACTGC 360
TCACCAGGTC CCCCAGGAAA CTCTACGCCC CTTTACAGTG TCACTGCTCA CCAGGTCCCC 420
CAGGAAACTC TACGCCCCTT TACAGTGTCA ACTGCTCACC AGGTCCCCCA GGAAACTCTA 480
CGCCCCTTTA CAGTGTCACT GCTCACCAGG TCCCCCAGGA AACTCTACGC CCCTTTACAG 540
TGTCACTGCT CACCAGGTCC CCCAGGAAAC TCTACGACCC TTTACAGTGT CACTGATCAC 600
CAGGTCCCCC AGGAAACTCC GCCCCTTTAC AGTGTCACTG CTCACCAGCC CCCCAGGAAA 660
CTCCGCCCCT TTACAGTGTC ACTGCTCACC AGCCCCCCAG GAAACTCCGC CCCTTTACAG 720
TGTCACTGCT CACCAGCCCC CCAGGAAACT CTGCCCCTTT ACAGTGTCAC TGCTCACCAG 780
TCCCCCCAGG AAACTCTGCC CCTTTACAGT GTCACTGCTC ACCAGGTCCC CCAGGAAACT 840
CCGCCCCTTT ACAGTGTCGC TGCTCACCAG CCCCCCCCAG GAAACTCCGC CCCTTTACAG 900
TATTGCTGCT CACCAGCCCC CCAGGAAACT CCGCCCCTTT ACAGTGTCGC TGCTCACCAG 960
CCCCCCCAGG AAACTCCGCC CCTTTACAGT GTTGCTGCTC ACCAGTCCCC CCCAGGAAAC 1020
TCCGCCCCTT TACAGTGTCG CTGCTCACCA GCCCCCCAGG AAACTCCGCC CCTTTACAGT 1080
GTCACTGCTC ACCAGCCCCC CAGGAAACTC CGCCCCTTTT GGGGCCAGAG ATGCTGTGAG 1140
AAGTGGCCTT TTATTATATA AAACTGTTTT ATGCAGAATT TAAGATGTAC ATGTGACCCC 1200
TGAGATTAAA CCACAGCCCC AAACAGCTCC CTGATTTTAG CCTTGTAGGA GACCCTGGGG 1260
CAGAGGGAAA CTGCTAAACC AGACTTGGAT TCCAGACCCA CCTGGAAGTC ATAAATGTGT 1320
GTTGTTTTAA GCCACTATAA TTTGGAGTCG TTTGTGACAC AGCAGAGCAA CAGATTACCA 1380
TCATGGTGTT GAAGGTAGAG CCAGCTGGGC TTGCTGGCTG ACTCCAGGGC ATTGGAGGAC 1440
GCCAGAGCAT TGACCTGAGC CCCTGGCAGG TGTGGCTGGC AGCATTGGGA CAAGGACAAC 1500
GAAGGCTGCA AGTCAAGAAC TCTGCGCTGG GGCCAGGCGG CGGCTCACAC CTGCAATCCC 1560
AGCACTGTGG GAGGCTGAGC CTGATGGATC ACCTGAGGTC AGGTTTGAGT TCAGCCTGCC 1620
CAACATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT TAGCCAGGCA TTGTGGTGCA 1680
TTCCTGTAAT CCCAGCTACT CAGGAGGCTG AGGCAGGAGA ATCACTTGAA CCCGGGAGGT 1740
GGAGGTTGCA GTGAGCTGAG ATCACACCAC TGCACTCCAG CCTGGGCAAA AGAGTGAGAC 1800
TCCATCACAA AAAAAAAAAG ACTTTGGATA AATATGTGTT GTCCAACAAC TTTGGATAAC 1860
AGAAAACACC ACAACAAGTT GAGAAATGGA TTACAGAAAA AAGAACGAGC TTCGTACGTT 1920
AGCACCTATA ATATCATTTC ATCCTGCATT TTGAACAATG AACCCTGAAT TCTCATGTGC 1980
GCTGGGCTCT GCAAATCATG TGGCTGCTCC CCATAGTCAG GAAGGAGAGT GGGACTCAGG 2040
GGAGGAGGCA GGATGAGCTG AGACCCAGGC TGCCTGTCCC TACCACTGAC CAGGACAGCG 2100
TTCCAGCCTC CCCGTCTGCT CAGAATCTGC CCTGACCTGC TCCACACCCC CGCAGGCCCG 2160
CAGGGGAGGG CAGAACTAGA AGGGACCAGC GCATAGGGAC CTGGGGGTGC TGGCACTGAG 2220
GTCTCTGGGC CTGGGATGCT GACCTTCCCG GAGCCCTGAG CTGGGCCAGG ACGAGGTCTT 2280
CCCATCAGAC TTGCCGCTGG CTAGGTGACC GGCCTGTCTC ACAGATGAAA ATATATTCTG 2340
AGGCCCAAAG GGGGCCCAGA CCCTGACTTT GTGGCCCAGA GCCAGGTTCT CCCCATAACC 2400
AGCAGGCTTC TTTACCCACA GGCCACTGTC CACCCAAGCC CCGCAGGCAG GAACCCTTGG 2460
TATTGGGTGG CCCTGAGCTT GGGATTTGCC GCTGGCTGTG TGGCCCTTCG GAGCCAGTCC 2520
GGCACACCCG CAGGCACACA CACATGCGCA CTCGCATACA GCCACAGATT ACACAGGCAC 2580
CAGCTTCCCG GGAATCCATT TGTCATGCAA ATGCCCCTCC TGGGGCCCCT 2630