EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-22253 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr5:131835300-131837560 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr5:131837047-131837066CAGCACCCCCTGCTGGCTA-7.03
GSCMA0648.1chr5:131836989-131836999GGGGATTAGC-6.02
Number of super-enhancer constituents: 40             
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_39368chr5:131835375-131836017Jurkat
SE_39368chr5:131836085-131837612Jurkat
SE_40726chr5:131829734-131835879Left_Ventricle
SE_40726chr5:131836212-131838737Left_Ventricle
SE_42103chr5:131829574-131839460Lung
SE_44054chr5:131830691-131837759MM1S
SE_47919chr5:131836298-131837089Pancreas
SE_47919chr5:131837194-131837965Pancreas
SE_48659chr5:131829847-131835640Right_Atrium
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_66244chr5:131835375-131836017Jurkat
SE_66244chr5:131836085-131837612Jurkat
SE_67186chr5:131830691-131837759MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr5131836369131837068
chr5131835833131835962
chr5131835332131835406
Number: 1             
IDChromosomeStartEnd
GH05I132493chr5131828971131839447
Enhancer Sequence
GGGTGCATAA TTGGGAGCAA AATGGACAAG GGTATGCTGG GAGCTCTAAG CCAGGAGGCC 60
TCTGGTGGCT AGTCACCTCC AGGAAGCAAA AGCCGTTATT TCTTCCTTGA GAATCCCCGT 120
GAATATTGGA GAGGGCTTCT CACAGCCCCA TGGGCTGGGG CATGAGTGTG TTATGCTTTG 180
CTTTTAGTGG AGGAGGTGAC TCCAGAAGGC TAAAGATTTA GGGACAGCTG ATGGTCCTGG 240
AATGCTTCTC AGCCTTGGGC CTACGCTGGG CCCTGTGAGG GGACTTAGAA GTAAGCACCG 300
TGGTCTCCAC TACTAACCTG CATGTGAGCT CTCCAAGGAC AGAGGATGCT CAGAACCACC 360
CCCACACCCC CACTCTGGCA CCCAGCACAT TGCTCTCAGG CAGTAGGCAC TTAGTAAGTG 420
TGCTCTGATT GCAGTGCCAG ACGTATGTCA TACCTCGAGT AAGAGGCAAA GAGGCAGAGA 480
TGCTGGGAGT ATGGAGACGG AGCAGGTTAT CTCAGTCATT GTTCACAGAT GGCTACTCTG 540
AGGAGGGGAC AGTTCAGCAA AGCCTCAAAG GATGAGTCAA AGGTTAATAG GCTAATAGTA 600
GGGGAGGGCA TTCCAGAACG TGAAAACAGC CCAAGGAAAG GCTTGGCAGC TCAGAAGTGC 660
AGAACGGATC TCGCTTTTGG TGTGGCCTGG AGTAGCTGCC CCAGAAGCTG AGGCTGGACC 720
AACCAGTAGG GGCCACACTC TGAAGAGCCT GGATGCTGTG CTCAAGAGTG GACTCTATCC 780
TGGTAGACAG AGGCCGCTCA GGGCTGGACT GATGTTGCCT TCCTTTCTGG AGCCAAGGCC 840
CAGACCAGGG TCTATCATCA GGTGTCTGTT GAATTAAATG CTAGGGCAGG TCTTGTGAGG 900
GCCACTGGTG GCCTGACCTA TGCTTTAGAA AACTTTCTGT GGCTGCTACA GAGGATTACG 960
CCTGTGGCAC ACCAGGGCAA GACTAGGGTG AGATAGTTTC CTAAAGGCAC AACATTTAAG 1020
GAGGTACTCG CTCTCAGGGG CCAACCCTAT ACTTGGGTGA GTCTGACGGT GAGTAGCTCC 1080
TTAAAGGTTT CACCCTAAGC ACCTGCCCTG CCTGCTTGCT CCACCCTATC TGGTCCCTTC 1140
TGCACACTGG AGGCTGGGAG GTAGACTAGA GGCAGCTCAA GTGATCCAGG CATATTAGGG 1200
CTGTGGCCAC AGGGGATAGA GATAGGCCTA GTTGAGAGCA GAATCAGATG ACAGGATTTG 1260
CCAGGACATG AGACTGGCTG GAGCAGGACC CATCCCCCCT CCCTGGGTGC CCCATTCTGG 1320
GAGAAGTGTA GGAGACCCCC CACTCTGCCT AGGAGTCTAT ATGTCCACAG CCAGGGCCAA 1380
AACAAGATCT TAGGCCTTGG CTTCTGTCCT AGGTTATGAG TCTAGGGAAC CAAGGACACT 1440
AAGCTAAAGA GAGTAGGGCA GCAGGTGAAA AAGCCACAGG CTGCCCCAGG AAGGCCCAGG 1500
CCACTGGAGA CCACAGCTAG AACCTACAAC CATGTCCCGA GACTGCTCGG CCTTGCCCTT 1560
TGGATGCTTG GGCACAGCAG GAAGGAAGTG ATAAGGGTGC CTCCACTGCT GGATGGGGCG 1620
TGTCTGTCAG TCCATCTTCC CCCCGCTGTC TGCCCAGCAA GACCAGGGGC CACCCCCAGG 1680
TGCTCCCCAG GGGATTAGCA GCTTGGTTCC CCAGCCCACA CCCCTAGAAG CTCTGACCCT 1740
ATGGCAACAG CACCCCCTGC TGGCTAATAT GGAAAACCAA CCCCTTTCCC TCCTCTAGCA 1800
GGCGGAAGTT TAGGGGTCTT GGAGAAAGAG AAGGGTGCAG GCACAATGCT GCGGGAAAGG 1860
GTGGGGGCAG GAATTCAGGA TGGACTTTGG CTATGGCAGA TAAGCAGGTG CCACCTGGTA 1920
AACAGAGCAC CTATTTCCTG ATCAGTAGCC TTTGAACAGA TGCCAGAGAG GCCAGGACAC 1980
AAGCAAAGGC AGAAATGGGG GTTTCTAAGG TAACTGCTGA GCGAGGCTGG CTCTCGTGGG 2040
AGTCCCTGCC TTCTCCTACA GCATCATGGC CCAGGAAGGC CTGCATCCTC TGTTGAGCAC 2100
TGTTCTCCTC AGGTGGGCTC AGGAACTCCC TCAGATTCCC CCTGAGCAAG CCACCTGGCC 2160
CCACAGAGGA TTTGGCCTAG GACTGAAGGC TGAGAGCTAG GCCTGAGACA GGGTAGTGCC 2220
CCAGGCACCC CAAAAAGAGG ATTTGTCCCT AAAATTCCTC 2260