EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS188-01158 
Organism
Homo sapiens 
Tissue/cell
Th2 
Coordinate
chr1:208003890-208007800 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs859711chr1208004898hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:208006828-208006846GGAAGGAAGACAGGAGGA+6.37
NFIAMA0670.1chr1:208004251-208004261GGTGCCAAGT+6.02
NFKB1MA0105.4chr1:208005402-208005415AGGGGATTCCCCA-6.71
NFKB1MA0105.4chr1:208005402-208005415AGGGGATTCCCCA+6.82
RARA(var.2)MA0730.1chr1:208005268-208005285TGACCTCTGTGTGACCA-6.3
ZNF263MA0528.1chr1:208006825-208006846AGAGGAAGGAAGACAGGAGGA+6.1
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_01610chr1:208003718-208006602Aorta
SE_01610chr1:208006681-208007933Aorta
SE_02940chr1:208003945-208006074Bladder
SE_03907chr1:208003545-208007521Brain_Anterior_Caudate
SE_06993chr1:208003570-208005482Brain_Hippocampus_Middle_150
SE_08580chr1:207991706-208006704Brain_Inferior_Temporal_Lobe
SE_09440chr1:208003916-208007804CD14
SE_10475chr1:208004630-208006320CD19_Primary
SE_11488chr1:207992533-208010277CD20
SE_12401chr1:208004637-208006256CD3
SE_13353chr1:208004754-208006344CD34_Primary_RO01536
SE_14644chr1:208004273-208007930CD4_Memory_Primary_7pool
SE_17929chr1:208003706-208007813CD4p_CD25-_CD45ROp_Memory
SE_18828chr1:207994794-208013240CD4p_CD25-_Il17-_PMAstim_Th
SE_20606chr1:208004352-208006469CD56
SE_24155chr1:208004812-208005329Colon_Crypt_2
SE_25829chr1:208003915-208006434Duodenum_Smooth_Muscle
SE_26666chr1:208003798-208005871Esophagus
SE_41597chr1:208003977-208004826LNCaP
SE_42138chr1:208003616-208008639Lung
SE_48593chr1:208003701-208006541Right_Atrium
SE_48593chr1:208006718-208012761Right_Atrium
SE_49524chr1:208003918-208005343Right_Ventricle
SE_50299chr1:208003929-208006142Sigmoid_Colon
SE_52485chr1:208003912-208006536Small_Intestine
SE_53314chr1:208003646-208008432Spleen
SE_54764chr1:207991828-208013085Stomach_Smooth_Muscle
SE_59011chr1:207980241-208007571Ly3
SE_61319chr1:207994376-208006461HBL1
SE_62794chr1:207980098-208006634Tonsil
SE_65312chr1:208003968-208004591Pancreatic_islets
SE_65312chr1:208004839-208005692Pancreatic_islets
SE_65312chr1:208005804-208008071Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1208006714208007152
Number: 1             
IDChromosomeStartEnd
GH01I207830chr1208003920208007544
Enhancer Sequence
AAGAAACAAA AATACAGAAA TCTAAGTATA TATAATCACA AAAAGTATGA GAATGTGCTC 60
GATGTTGGGG TGGGGACAGA AATGGTACTC ATAGAGTAGA AGTCTGATGG CATTCATGGG 120
GAAAAGGCTC CTAAGGAGCA GTGCCATTAA TAGTTGCAGA CCAACAGCAG TGATCATGGT 180
GTGGTCAGAC CTCAGCCATG AAGACCACAC TGTGCCAGTC TCCTGGAGGA ACTACCCCAG 240
AGCCACTGAG GAGCTTTCCC CCAACCCAAG AGACCATGAC ACTTCCACCC ATGTCACTGA 300
GCTGAAGCGA AACAAGGCCC AGCAGTGACA ACGAACACTC CAAGGACACA ATGCAGTGCC 360
AGGTGCCAAG TGAAAATCCG AGAGGCAAGG GCTGGGGACA GCCTGTGCTG GAGGGTAGGT 420
TCTGGCAGAG GTGAAATGCA GACACACACT CAGAATGCCG CCACAGACAG GGAGCCGGAG 480
CCAGGCGGCA GAGAGTGAGT GACCTGGCAG ACGCTGGCCA AGAACACAGG GCTCCCCGAC 540
CCTCAGGGTA AAGGAAGACA AGCAAAGGCC AAGTTGAGTG CTGAATTCAC AGCACAAATG 600
GAAGTGAACC CCAGCACCAA CAGGGACTCC CGTGTGAAAT ACGCCCAAGG GCTGCACAGA 660
GAGGGGCATG TTTGCATGGG GGAAGGTCAG GCCTGCAACA GCAGATATTG TGACTAGGAT 720
GCTCTGTTTG TAAGTAGATG CTTTTTCCTG GACAGACACA GTCAGTCTGT CTCTCAGGCC 780
AGAAATCCAG GCTCCAAAAT GTCCTGCCCA AGCTGGCTCC CATCACCTCT TGGGAAAGTG 840
AAACAGGCCA AAACATCTAT CTTGTCTTAG GCCGCTAATC ATTAAATCTA AGCTCCCACC 900
CCAGAGGGCT CACAACTCAG CCATAAGCAA AACCCAGACT GGCAATAGCA CTGGCACCTG 960
CTATCCTGAC TATGGGCTGG GGCTGAGTGA ATGTGGCCAC TCTGCTAACC ACTGGTCACA 1020
GCTCCTGCTG CCTAAAATAC AGGAGGACAA AGTCTTCTTG GGACTGAGGG AGTAACCCAA 1080
TGTGCCTCTT GGCTGGCTGC TCAAAATCTT GGCCCTGCCA ATGGATGGAA ATAATTTCCA 1140
GAGAGACAGA GTGTGGTTGG GCCATGTGAG AGGGACTTGA GGAGAACATT ACTCCATTCC 1200
TCAACAGCGG AACCTGTAGC CTGTGCCAGG CCAGACATGG CCGGGATTGA GGGGTCTTGG 1260
CCAGACTCCC TCCAGGCACA GGTTGGTGCC CTCAGACGCT GCTGCTGCTC TTGTGGGCAG 1320
GAGGAGATGT CTCTAGGGTA GGAAGAACCT AGGCCTCTGA TGATTTATGG GTCTGTGCTG 1380
ACCTCTGTGT GACCACATGG GTTTAGCACC ATGTGACTTA AAAATGGAGT CGCTTTCCTG 1440
CCTCACAACA AACTTCTGCT CTACTTAACT GAGTCAGATC TAGACAGCAG GAATCATAAA 1500
CACAAGTGGG GCAGGGGATT CCCCAAACAC TTCTGACTTG AACTTTCATT TCCATACTGC 1560
CTTATCCCCC AAGCAGGGGC ACGTCCGTAC CTGCAGCCTA GGACAGAGGA GAAAAGAGAC 1620
CAGGGCCATT ATGCATGGCC TGGGTGCAGG TCCGAGCTTT CAGCAAAGTG CCAGCTTTGC 1680
CAGGAGCAGG GACAAAACTT CCAGGGCCGA GACTCTCATT CAGGGGTGGG AGAGGAGCTG 1740
GGGACTGTCT AAAACATAAC AGTTAATATT TGGGATACGT TTTCATAATG TGAAACCATA 1800
CCAAAAGTAA AGTTCCACAA AACCTTTGAT GATGTGAATA CTTCCTCTGC ACTGGGAGGG 1860
GATGTTGACC AGAATCTTTG GGGGTGGGAG GCAGTCCTGT GGTTGATTTA TTTACTGAAG 1920
GTAGGTGTTG GAATTACACT CTTTTAGAGG GTTCAGCTCT CTGAAACCCC CTGGGACCAC 1980
TGGACAGCCA TTATTCTCAG GCTAGGATTT GACATAGGCC TCCGAGGCCA ATGTTCTTTC 2040
TCCAAAAGCA GCACAGCAAC AACAGCTCTG CCTTAAAAGA CAGAAGATTA CACTTAGAAG 2100
ATTTCTCCAA CGCCACATAC TTTGGAGGTG AGAGGAGTAC CCCATCACTC TCCCTCTGAA 2160
AACTTCAAAA CCTTCAGAGG CCAGGGTGAA TATTTAGAAA GCAGGCGGGT CCAACAGAAA 2220
GAACGGCCAT TGATCTATTC CAAAAAAATA ATGTGTTTGG GGCCCATGTG TCAGGTACAG 2280
CGCGAGGCAC TTTTTAAGGA GCTCCACCCT TGGCTGGCAG GAACTCCCTC GGTCAGCAGA 2340
GGCTGGTAAA CTAAGAAAGC AAGATGCTAG GAGGACAGCT GGCTCCTTAA TCCCACCCTG 2400
GCCCCCCAAA CAAGACAGCT CAAGTCTTGC CGGCCCTGGA GGCCCAGGCA CTTGGACATC 2460
ACTTGCTCTA TGCCTTTCTT GGGAGGCAGA GCTTAGTGGG GGTTGAGGAG AGATCTACAG 2520
GCTGAGTGCG CTCATGACAC AATCAAGAAG TTTCTGGGGC CAGGTGCGGT GGCTCACGCC 2580
TGTAATTCCA GCACTTTGGG AGGCCAAAAG AAGCCAAGGC GGGCAAATCA CTTGAGGCCA 2640
GGAGTTTAAG ACCAGCCTGG CTGACATGGT GAAACCCCAT CTCTACTAAA ATTACAAAAG 2700
TTATCTGAGC ATGGTGGCAC ATGCCTGTAA TCCCAGCTAC TTGGGAGGTT GAGTCATGAG 2760
AATCGCTTGA GCCTGGGAGG TGGAGGTTGC AGTGAGCCAA GATTGTGCCA TTGTACTCCA 2820
GCCTGGGTAA CAGAGCGAGA CTCTGTCTCA AAAAATATAT ATATAAGTTT CTGGGTAGGC 2880
TGACATGAAA AAATTACCAC TGGAGCTTCT GAGAGCCCTA AATCACCATA AGGGTAGAGG 2940
AAGGAAGACA GGAGGAACTG AGATGCTGAG ATAAGCTGGG ATGTCCCAGC CCACTTCCCT 3000
AGAGAGGCCC TTTCCTAACA GCCAGCGGGA GAACCCTGTT CACGGAGCCC TATCACTGAC 3060
CTCGAGGGCA GCACCAGCAT CCACAGTCAG GTCATCCCGA GAGTCGTAAC CACTGTTCCT 3120
GCCCCAAACC CAATGACCCT CTCAACCCCA TCCAAATAGC CCAGGATGAG CCACAAGACA 3180
GGGCCTTAGA ACCCTGGGGG TGTAAGACAC CCTGAATGTC ATCTGGCCTC ACCTTCCACT 3240
GAGACAAGAA GATTCCGCCT TGGGTTAGAG TCCAAGGTGT GGGATCTTGG GTGAGTTATT 3300
CCATGTCTTG CCTAAATTCT CTCATCTATA AAGTAGGGCT GATAAGCTCA TCATACCTCT 3360
TCACAGTGTT GCTGTGAAGA TTAGAGTCTA TTTGAGTAAA GCACTCAGCA ACAGTGCCTG 3420
GTACCCAACA AGTATTCAGT AAGGAAAGTT ATGGCTACTG TTTTCATTAT TAGCACCCCT 3480
GCATGGTGGA CATTCGCTCA TGTGTAAACA CTACAGGGCC CACGGAAGGA GCTGGAGACC 3540
TGACAGGGTC ACCCATCTTC TCTCCCTCAC ATCCTTCACA GCCCATAAAG CAAGACAGGA 3600
ATCCAGCTCC CAACACCAAC GTCTGCCTCC CTGTCACAGC TACCCACTGG CCCCAGGGCT 3660
GCCCCCTGAG GTACCACAGG GTAACTCTGA CACCCACATC ACCTGACAGT GCTTTAAGCA 3720
CACAATACTG TACCTAGCAA ACCCCCTCTC ACCAAAATCT CTACCTCTCT GGGCCACGCA 3780
GTCTCATGTT TTTAACCACT CTTCACGTGC CAGCAGCTCT GCTCTGTACT TCAACTAGTA 3840
GTTTGACATT TTCCCTCCTA ATTGAGATCA GGAACTGGAG CGGCCCTCCA AAAGTGGCCT 3900
GAGAAGGCCA 3910