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

TagContent
EnhancerAtlas ID
HS104-48577 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr5:131835930-131838840 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr5:131837047-131837066CAGCACCCCCTGCTGGCTA-7.03
ELF5MA0136.2chr5:131838417-131838428ACCAGGAAGTA+6.02
GSCMA0648.1chr5:131836989-131836999GGGGATTAGC-6.02
STAT3MA0144.2chr5:131837850-131837861CTTCCCAGAAA-6.02
Stat4MA0518.1chr5:131837847-131837861CCACTTCCCAGAAA-6.14
YY1MA0095.2chr5:131838127-131838139GCAGCCATCTTG-6.74
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00037chr5:131820679-131837440Adipose_Nuclei
SE_04124chr5:131835240-131837326Brain_Anterior_Caudate
SE_06435chr5:131828999-131837748Brain_Hippocampus_Middle
SE_10340chr5:131835704-131837777CD19_Primary
SE_10915chr5:131818633-131838738CD20
SE_13479chr5:131836174-131839047CD34_Primary_RO01536
SE_17370chr5:131818848-131837330CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131818558-131837415CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131818792-131837424CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131836302-131837314CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131828783-131837777CD56
SE_22284chr5:131818534-131837164CD8_primiary
SE_23079chr5:131830842-131839811Colon_Crypt_1
SE_23750chr5:131835068-131838981Colon_Crypt_2
SE_25340chr5:131835682-131838025DND41
SE_25784chr5:131828604-131839493Duodenum_Smooth_Muscle
SE_26597chr5:131834716-131837077Esophagus
SE_27629chr5:131830752-131839506Fetal_Intestine
SE_28559chr5:131830527-131839276Fetal_Intestine_Large
SE_31393chr5:131829777-131839489Gastric
SE_39368chr5:131836085-131837612Jurkat
SE_40726chr5:131836212-131838737Left_Ventricle
SE_42103chr5:131829574-131839460Lung
SE_44054chr5:131830691-131837759MM1S
SE_47919chr5:131836298-131837089Pancreas
SE_47919chr5:131837194-131837965Pancreas
SE_48659chr5:131835953-131838663Right_Atrium
SE_50051chr5:131828811-131839642Sigmoid_Colon
SE_52336chr5:131828839-131839793Small_Intestine
SE_53285chr5:131829513-131839339Spleen
SE_54554chr5:131829395-131838583Stomach_Smooth_Muscle
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131835327-131838706Pancreatic_islets
SE_66244chr5:131836085-131837612Jurkat
SE_67186chr5:131830691-131837759MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5131838348131838647
chr5131836369131837068
Number: 1             
IDChromosomeStartEnd
GH05I132493chr5131828971131839447
Enhancer Sequence
CCAAGGAAAG GCTTGGCAGC TCAGAAGTGC AGAACGGATC TCGCTTTTGG TGTGGCCTGG 60
AGTAGCTGCC CCAGAAGCTG AGGCTGGACC AACCAGTAGG GGCCACACTC TGAAGAGCCT 120
GGATGCTGTG CTCAAGAGTG GACTCTATCC TGGTAGACAG AGGCCGCTCA GGGCTGGACT 180
GATGTTGCCT TCCTTTCTGG AGCCAAGGCC CAGACCAGGG TCTATCATCA GGTGTCTGTT 240
GAATTAAATG CTAGGGCAGG TCTTGTGAGG GCCACTGGTG GCCTGACCTA TGCTTTAGAA 300
AACTTTCTGT GGCTGCTACA GAGGATTACG CCTGTGGCAC ACCAGGGCAA GACTAGGGTG 360
AGATAGTTTC CTAAAGGCAC AACATTTAAG GAGGTACTCG CTCTCAGGGG CCAACCCTAT 420
ACTTGGGTGA GTCTGACGGT GAGTAGCTCC TTAAAGGTTT CACCCTAAGC ACCTGCCCTG 480
CCTGCTTGCT CCACCCTATC TGGTCCCTTC TGCACACTGG AGGCTGGGAG GTAGACTAGA 540
GGCAGCTCAA GTGATCCAGG CATATTAGGG CTGTGGCCAC AGGGGATAGA GATAGGCCTA 600
GTTGAGAGCA GAATCAGATG ACAGGATTTG CCAGGACATG AGACTGGCTG GAGCAGGACC 660
CATCCCCCCT CCCTGGGTGC CCCATTCTGG GAGAAGTGTA GGAGACCCCC CACTCTGCCT 720
AGGAGTCTAT ATGTCCACAG CCAGGGCCAA AACAAGATCT TAGGCCTTGG CTTCTGTCCT 780
AGGTTATGAG TCTAGGGAAC CAAGGACACT AAGCTAAAGA GAGTAGGGCA GCAGGTGAAA 840
AAGCCACAGG CTGCCCCAGG AAGGCCCAGG CCACTGGAGA CCACAGCTAG AACCTACAAC 900
CATGTCCCGA GACTGCTCGG CCTTGCCCTT TGGATGCTTG GGCACAGCAG GAAGGAAGTG 960
ATAAGGGTGC CTCCACTGCT GGATGGGGCG TGTCTGTCAG TCCATCTTCC CCCCGCTGTC 1020
TGCCCAGCAA GACCAGGGGC CACCCCCAGG TGCTCCCCAG GGGATTAGCA GCTTGGTTCC 1080
CCAGCCCACA CCCCTAGAAG CTCTGACCCT ATGGCAACAG CACCCCCTGC TGGCTAATAT 1140
GGAAAACCAA CCCCTTTCCC TCCTCTAGCA GGCGGAAGTT TAGGGGTCTT GGAGAAAGAG 1200
AAGGGTGCAG GCACAATGCT GCGGGAAAGG GTGGGGGCAG GAATTCAGGA TGGACTTTGG 1260
CTATGGCAGA TAAGCAGGTG CCACCTGGTA AACAGAGCAC CTATTTCCTG ATCAGTAGCC 1320
TTTGAACAGA TGCCAGAGAG GCCAGGACAC AAGCAAAGGC AGAAATGGGG GTTTCTAAGG 1380
TAACTGCTGA GCGAGGCTGG CTCTCGTGGG AGTCCCTGCC TTCTCCTACA GCATCATGGC 1440
CCAGGAAGGC CTGCATCCTC TGTTGAGCAC TGTTCTCCTC AGGTGGGCTC AGGAACTCCC 1500
TCAGATTCCC CCTGAGCAAG CCACCTGGCC CCACAGAGGA TTTGGCCTAG GACTGAAGGC 1560
TGAGAGCTAG GCCTGAGACA GGGTAGTGCC CCAGGCACCC CAAAAAGAGG ATTTGTCCCT 1620
AAAATTCCTC CCGCAACTAT CCAAGGCTAG GAATAGAGGC AGGGACACAT CAGCAGAACA 1680
AAATCTCAGA GCGTCCCTGA GCAGCTGCCT GGCTCTTCAG ATGCAAACCT GGTTAGACAC 1740
ACACTTCTCC TGAGCTCTAG GCCCATGGCT CAGGCACAAG GACCACCTCG GAGTGCTGGA 1800
TGAGGTGCCC AGTGGACAGA GGAGTGAGAG GACCCAGTGT ATGCCACTTT GACCCTTCAG 1860
CTGTGAGCCA GGAAGTCCAG GCAGACACAG CCACAAGCAG GGCCATGCCC TGGGCAGCCA 1920
CTTCCCAGAA AAGTTTCTGC CGCAAAACAG AGAGAGTGGC CTTCCCTGCC CTGCATGACC 1980
CTGGCACCTG GAGTCCTCAC CTCAGATAAG AAGCCAGTAG TTCTAGGAGT TTACTTACAT 2040
CATGGCTCTT GATTACAGTG AAGACCGGGG CCTTGCCCTA CCCCAGGGAA ACTTCTCTCC 2100
CGGGCCAATG GTGTGGATGG CTGCTGTTCT CTTATGACTC AGTGTGGGCC TGGTGCTCAG 2160
GAGAGCTGCT CCTTCCCATG CCCTGGATGT GAGCTCAGCA GCCATCTTGA TTCACCAGGA 2220
CAATGTGAGC TCCACACACC ACCCTCAGAC CCTCACCTAC CGGGCTCTCA GGGAGAGATG 2280
AGGCCTCCCG GAGAGTCCAC AAAGAGAAAA AAGCGGCTTG GCTGCCAAAA CTGCCCACGC 2340
ACCCCAGATG CCATGCTCAG CTAGCAGCCC TGGTGCCACA CAGCCTGAGA GCAGGTGGGA 2400
GCCATAGATG CAACAAGCTG TCATCAGGCA TGGGAGGGCT GGGCTGCCAT GCTGAGGCTG 2460
GTGGGGTGGG AAAATCAACT TGCAGCCACC AGGAAGTACA GGAGCAGAGT AAACAACAGT 2520
TGAGGTCAAA AGGGTCCAAT TTCCTTGGAC AAGCAGGCCT CAAGAAGGCC TCTGAGCTGC 2580
ACTGCCAACT GTATTGTATT CTTGTGTGTG TTCTGTGTGA ACCTAACACC CCCGGCGGCC 2640
AAGGGAAGCC CCTTGGCCCT CCCTTGGGTG GCAGCCAACA CTAGGACCAG AGAAGTGGCA 2700
GTTGTGTCAT AAAGTTCCCA AGACACTTCT GGAGGAATCA ATCTTCTTTT TTAGTCTTCT 2760
CTGCTCATTT TTTCTTGTCA TTTTCCTGTA TGTGTATCTT TTCCCTCTCT CTTCTAGCCC 2820
AGAAATGCTT ATTGACCACT GGTGGCCTAT TGGGAGTGGA TTACTTGACA CATTCACATT 2880
TACTCTGTGC CCAGATGCTA GGCACAGAAG 2910