EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-06138 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr13:114886020-114888810 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr13:114887118-114887133CGACCTTTGACCTTC-6.59
Nr2f6MA0677.1chr13:114887118-114887132CGACCTTTGACCTT-7.25
RxraMA0512.2chr13:114887118-114887132CGACCTTTGACCTT-6.93
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_02428chr13:114885780-114886826Astrocytes
SE_06573chr13:114885807-114890011Brain_Hippocampus_Middle
SE_11986chr13:114885993-114886605CD3
SE_14520chr13:114885691-114887152CD4_Memory_Primary_7pool
SE_15834chr13:114885890-114886808CD4_Naive_Primary_7pool
SE_15834chr13:114887971-114888932CD4_Naive_Primary_7pool
SE_17059chr13:114885939-114886553CD4p_CD225int_CD127p_Tmem
SE_17352chr13:114883523-114898593CD4p_CD25-_CD45RAp_Naive
SE_17971chr13:114885782-114887513CD4p_CD25-_CD45ROp_Memory
SE_18337chr13:114885848-114898460CD4p_CD25-_Il17-_PMAstim_Th
SE_19216chr13:114885757-114888693CD4p_CD25-_Il17p_PMAstim_Th17
SE_20430chr13:114885957-114886898CD56
SE_21920chr13:114885877-114888378CD8_Naive_8pool
SE_21920chr13:114888408-114891140CD8_Naive_8pool
SE_22425chr13:114885910-114887185CD8_primiary
SE_22425chr13:114887206-114888527CD8_primiary
SE_29941chr13:114885767-114888711Fetal_Muscle
SE_31056chr13:114887075-114889022Fetal_Thymus
SE_32435chr13:114886020-114886755Gastric
SE_32435chr13:114886879-114887645Gastric
SE_37803chr13:114882968-114887163HSMMtube
SE_38174chr13:114882988-114888488HUVEC
SE_38982chr13:114885840-114886777IMR90
SE_43224chr13:114885977-114889389Lung
SE_44466chr13:114885953-114887352NHDF-Ad
SE_44821chr13:114885842-114886973NHLF
SE_44821chr13:114888029-114889321NHLF
SE_46527chr13:114885929-114886915Osteoblasts
SE_47322chr13:114885849-114891322Panc1
SE_50252chr13:114885977-114889418Sigmoid_Colon
SE_52117chr13:114885965-114887323Skeletal_Muscle_Myoblast
SE_52117chr13:114888152-114889257Skeletal_Muscle_Myoblast
SE_53247chr13:114885985-114887600Small_Intestine
SE_54100chr13:114885966-114889031Spleen
SE_56179chr13:114886013-114886868u87
SE_62671chr13:114874284-114928516Tonsil
SE_63914chr13:114885951-114887337HSMM
SE_63914chr13:114888152-114889260HSMM
SE_67713chr13:114886013-114886868u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr13114886941114887983
chr13114886931114887638
chr13114888563114888689
Number: 1             
IDChromosomeStartEnd
GH13I114117chr13114882921114891675
Enhancer Sequence
CTCCAGCCAG GCGTCGATCA GGGCCCTCCC TCCTCTCTCC AGCCAGACGT CGGTCAGGGC 60
CCCTCCCTCT CTCCAGCCAG GCATCAATGC CGTTCAAGGG GTCTGGACCA ACAAGCCCTG 120
GTGGAGAACA ATCCCCACAG AGAAACTCCG TGTGACCCTG CCCCACAGAT AACACGGAAA 180
GGGACTTTTC ATGGTCAGAA CCTACTGATC TAGAAGTGAT CAAACACTCT CTTCTCCTGA 240
CTTCCTGTCA CCAGGCACGG GTGAGGAGGA ACACCAGCAA TTTCTTACTA ATTACGGCTC 300
AAGCACCAAT GTTTGTCCAC CGTTTTCTTC TCACACAGAT CTAAGAGGAT CAAGATGATT 360
CCCAGAGTAA CATCTGTCTC ATTTGAATTC CAGTGTGCTT CCCCGAGTGG CACAGCCGAG 420
CTAGTCTTGG GCTCTGGAAC AGTCCAAAGA CTGGGGACTC CCCTGTAACA TGCAGCCACC 480
TAAGAGAACA GGTCAGTGAC AAGTAGGGGG AAAAGCTATT AGGAAAAAGA ACAAGTTGTG 540
GGCCTAAAAA CAAGATGTTT CTTATACAAA TACAAAATAC TAGAAAATTG CACAGCAGTT 600
GCCAGAAAAG ATCCCAAGTT GTGGAAAGTA GAAAGGCAGG TGCATCCCAG CACTGCGGCC 660
GGGGGCAGGA GGCCACCCGC GGGGCATTCG GACCCCCGTG CCCCAAACAC ATCCCGCCGA 720
GCCTCCTGGG ACCAGGCCCC TGAGAGCCAC GGGGCTGTCT GGAGAGTGTC CCCAGCCTCA 780
GCCATGTGGG GTAGAATAAA AATGATTAAG AACTGCTTGA GAAGTTTTAA ACTGCATGCA 840
GCCTACTCAG CACAGATTGG CCCGTGTCTT CTGCCACGGA TCTCGGCTAA AGGAAAAGCC 900
AACAGAAGCC CACCGGAGCC TCCCTTACCT CCACCCAACA CTGCACATCA AGCCGTGCAA 960
CCCTGCCCCA AACGGTCCCA GGGTCATGGG TGTGCATACA TGTGCATGTG TGCAAGCATG 1020
TCACAAGAGG AGACCTCCGA GGAACATAAG GATGCGGACT CCTCCCTCAG CCTGAACCTC 1080
TGTCTCTCAG GCACAGCTCG ACCTTTGACC TTCGGCTTCC CCAGAGAAAG ACTTTGAACG 1140
CTTCACTCCT CTGTAGCCCT GAGGACGCGG GCGGCCAGAC CAGTCCCTGA GTGCGGCACC 1200
ATGGCCGTGT GAGTTTATGG CCCATTGCGC TAGCCCTGTA CAGTGAATGA GATACTAGTT 1260
GTTTACAGCT GTGAGCATAC ACAGGCCCCC CGCCACACGC TCAGGAAGGA GCTTCTCGGA 1320
ATCTCTCTCC TGCCTCGCAC CATGCAGCCG GGCTAGCAGG TTTGTGGGCC GAGTGCAGGA 1380
GCCTGCTCCC ACTGTCACTG CAGGTGACTG GCTGAGGGGC ACACAGGGCC CAGAGGCTCC 1440
TACCTCCAGC CACCGCCCCT AAACTAATGA AGATTCCAGT CCGTGGGGCC CACCGCAAAT 1500
CCCAGAATCT CAGCAGTCAG TCTTGGACAT TAGTTGTCGG GGAGGGAGAG GATCTGGGAG 1560
GCCAGGCGTC CCTTCCAGGC TGCGCAGCCG GCCACGGCGG CAGAGCTTCC CCAGGCTGCT 1620
CCAGCCTTCA GGGCCCCTCC GCGGTCAGCC CCACCCCCGG CCAGCAAGGC TTCCTGAGAA 1680
GGCTGAGCTT GGCACCTACA GACTGGGGGG GATCTGGAAT TCCCCAGAAA AGCCCTCATC 1740
CCAAAGCCCA TGGGAAAACC AGCCCTGTTG GAGCATCCCA CCCGGACCTC GGAGGAGAGT 1800
CCGGCATGGC CAGTCCCCTG GGCTCTGCAT GCAGATGGTT TTCCCAGAAC CGGTTCCTCT 1860
TCCTGAATCT CTGCTAATGG CCCTGTCCAT CAGTCTGACC CCAGCCTTGG AAACCCCCAT 1920
GCAGCCTGGG CCAGAATGAA GTAGGCAACC AGAGGCTCAG GGTGCTTGGG GCCGAACCAC 1980
CCCCAGCTCC ACCACCTCCT TCCTGCCCCC GAGCCGTGCC TTCCCCCGCT GGGTGGGCTT 2040
GCTCTGCATC TGGGAGCACC TGGGCCCGGG GGTGCAGGTG GGTTCGCCCC TGCCCATTGG 2100
AGGGAAATGT TCTGACATGG AAGCAGAGGG CACAGCATTC AGGAGAACCA GTGGGGCCTC 2160
CACACAGGGG GACGCAGCTA GGAAGGGGGT CTCCGGCCGG TCGGCCCCGA GTGAGGGACG 2220
CAGCTAGGAA GGGGGTCTCC GGCAGGTCGG CCCCAGCCCT GACTCCAGGC CTGTGCATCT 2280
CACTGCTGCC CAAAGCAAGG ACCACTGGCT GCCATGACAG CTGCCACAGT GCTGAGCAGG 2340
CCCAGCCAAC GCTGCATGAG AAAGGGCTCT AGGAAGGAAA AGGCCGCGGC AGCACCCAGC 2400
CTCCTTTCTG AGGAAGCGAT TCCACGAGCC ACAAAAGCGC CTGGGCTGTG GTCATCAGAG 2460
TCCACCACAA GACAACCTTC CTGGGTCCCT ACACCCTGGA CACACCTTCG GTGCGTGCCC 2520
GGCATGGAGA CGCTCCTGCT GCCGGCATGG CTTTGGGGAC AGCACTTTGC TCCTGGAGCC 2580
TCAGAGGAGG GGGGCCGGAA ACATGTGTCC TGCACAGTCA CCACCGGACG CCGAGGTGGC 2640
CGCCCCAGCA GGGGCCATGG GCTGAGGCTG GTCCTCAGGC TCCCAGAGCA ATGGCTGCTC 2700
TGGGGAAGAG AAAACACAGA AGTGACAAGA TCAAGGCAAA CTAGCTGCTC CAGCACCTCG 2760
AGGGTTTGGA ACCAAAACAA GAAATCTCCA 2790