EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-32628 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr5:131836240-131837540 
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: 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: 1             
ChromosomeStartEnd
chr5131836369131837068
Number: 1             
IDChromosomeStartEnd
GH05I132493chr5131828971131839447
Enhancer Sequence
GGCTGCTACA GAGGATTACG CCTGTGGCAC ACCAGGGCAA GACTAGGGTG AGATAGTTTC 60
CTAAAGGCAC AACATTTAAG GAGGTACTCG CTCTCAGGGG CCAACCCTAT ACTTGGGTGA 120
GTCTGACGGT GAGTAGCTCC TTAAAGGTTT CACCCTAAGC ACCTGCCCTG CCTGCTTGCT 180
CCACCCTATC TGGTCCCTTC TGCACACTGG AGGCTGGGAG GTAGACTAGA GGCAGCTCAA 240
GTGATCCAGG CATATTAGGG CTGTGGCCAC AGGGGATAGA GATAGGCCTA GTTGAGAGCA 300
GAATCAGATG ACAGGATTTG CCAGGACATG AGACTGGCTG GAGCAGGACC CATCCCCCCT 360
CCCTGGGTGC CCCATTCTGG GAGAAGTGTA GGAGACCCCC CACTCTGCCT AGGAGTCTAT 420
ATGTCCACAG CCAGGGCCAA AACAAGATCT TAGGCCTTGG CTTCTGTCCT AGGTTATGAG 480
TCTAGGGAAC CAAGGACACT AAGCTAAAGA GAGTAGGGCA GCAGGTGAAA AAGCCACAGG 540
CTGCCCCAGG AAGGCCCAGG CCACTGGAGA CCACAGCTAG AACCTACAAC CATGTCCCGA 600
GACTGCTCGG CCTTGCCCTT TGGATGCTTG GGCACAGCAG GAAGGAAGTG ATAAGGGTGC 660
CTCCACTGCT GGATGGGGCG TGTCTGTCAG TCCATCTTCC CCCCGCTGTC TGCCCAGCAA 720
GACCAGGGGC CACCCCCAGG TGCTCCCCAG GGGATTAGCA GCTTGGTTCC CCAGCCCACA 780
CCCCTAGAAG CTCTGACCCT ATGGCAACAG CACCCCCTGC TGGCTAATAT GGAAAACCAA 840
CCCCTTTCCC TCCTCTAGCA GGCGGAAGTT TAGGGGTCTT GGAGAAAGAG AAGGGTGCAG 900
GCACAATGCT GCGGGAAAGG GTGGGGGCAG GAATTCAGGA TGGACTTTGG CTATGGCAGA 960
TAAGCAGGTG CCACCTGGTA AACAGAGCAC CTATTTCCTG ATCAGTAGCC TTTGAACAGA 1020
TGCCAGAGAG GCCAGGACAC AAGCAAAGGC AGAAATGGGG GTTTCTAAGG TAACTGCTGA 1080
GCGAGGCTGG CTCTCGTGGG AGTCCCTGCC TTCTCCTACA GCATCATGGC CCAGGAAGGC 1140
CTGCATCCTC TGTTGAGCAC TGTTCTCCTC AGGTGGGCTC AGGAACTCCC TCAGATTCCC 1200
CCTGAGCAAG CCACCTGGCC CCACAGAGGA TTTGGCCTAG GACTGAAGGC TGAGAGCTAG 1260
GCCTGAGACA GGGTAGTGCC CCAGGCACCC CAAAAAGAGG 1300