EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS040-14869 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr17:17729140-17731490 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr17:17729430-17729447GGAATTCTGGGAAAGCA-6.1
FOSL1MA0477.1chr17:17729208-17729219CATGAGTCACC-6.62
JUNDMA0491.1chr17:17729208-17729219CATGAGTCACC-6.02
SP8MA0747.1chr17:17730446-17730458AGTGGGCGTGGG-6.14
ZNF263MA0528.1chr17:17729948-17729969TCCTCTTCCCTCTTCTTCTTC-6.3
ZNF263MA0528.1chr17:17729952-17729973CTTCCCTCTTCTTCTTCCTCT-6.73
ZNF263MA0528.1chr17:17729945-17729966TCCTCCTCTTCCCTCTTCTTC-6.75
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00881chr17:17727083-17731669Adrenal_Gland
SE_02989chr17:17729165-17730191Bladder
SE_06389chr17:17714600-17732045Brain_Hippocampus_Middle
SE_12214chr17:17729217-17730344CD3
SE_14781chr17:17723184-17730304CD4_Memory_Primary_7pool
SE_17733chr17:17725350-17731822CD4p_CD25-_CD45RAp_Naive
SE_20996chr17:17729210-17730456CD8_Memory_7pool
SE_22841chr17:17727091-17730952CD8_primiary
SE_23173chr17:17729000-17732088Colon_Crypt_1
SE_23799chr17:17729161-17730256Colon_Crypt_2
SE_24725chr17:17724801-17730019Colon_Crypt_3
SE_24725chr17:17730094-17731708Colon_Crypt_3
SE_26625chr17:17720649-17731613Esophagus
SE_27885chr17:17727076-17730457Fetal_Intestine
SE_28899chr17:17727037-17730445Fetal_Intestine_Large
SE_31441chr17:17724607-17731734Gastric
SE_34007chr17:17727154-17731941HCC1954
SE_34262chr17:17727051-17732342HCT-116
SE_34795chr17:17727093-17730805HeLa
SE_36316chr17:17727079-17730243HMEC
SE_39928chr17:17727115-17730848K562
SE_42125chr17:17727048-17730383Lung
SE_48150chr17:17721465-17732285Psoas_Muscle
SE_50203chr17:17720773-17732067Sigmoid_Colon
SE_51164chr17:17723081-17731665Skeletal_Muscle
SE_52449chr17:17727010-17730923Small_Intestine
SE_54926chr17:17727086-17730019Stomach_Smooth_Muscle
SE_57042chr17:17729154-17730558VACO_400
SE_57042chr17:17731020-17731967VACO_400
SE_60863chr17:17723038-17753684DHL6
SE_61850chr17:17725940-17761172Toledo
SE_62888chr17:17723024-17755643Tonsil
SE_63332chr17:17727040-17744985NCI-H82
SE_64851chr17:17729049-17730247NHEK
SE_65718chr17:17713037-17732290Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr171772994717730262
chr171773115317731443
Enhancer Sequence
GCTGGTCTCG AACTCCTGAC CTCAGGTGAT CCTCCCACCT CGGCCTCCCA ATGTGTTGCG 60
ATTACAGGCA TGAGTCACCG TGCCAATTTC TGTGGAAGCT GGTCACCAGG TTAAGACTGA 120
AAAAGGAAAC TCTAGAGCCA GCCCTGCAGC CTCCCTCAGA GACACACCCA AGTGGGCTAT 180
CTGGGGCTGC ATGCCAGGCC CTGCTCTTCC TTTAGCCCCT CCCTTGCTGT GTGATGGGGA 240
CAGTCCACTC CCCACCCTCT GAGCTCCCAC ACCTACGATC TCCAGAGGTG GGAATTCTGG 300
GAAAGCAAGT GTGTAAAACA TCCATCACTC AACAGTCTCA ACAAAGGTTA GTTCTCTCTA 360
CAGCAATTAG AATGGTTTAG AACTGGAAAG TCAGGTAGTG AGTTGCCTGA TACTTGCAGT 420
ATTCACGTTG GAGCTCCATT ACCATTCGAC TGAGTCTTTT TTTTTTTTTT TTTAAGGGGA 480
GTTAACGGGG CCAGTCTAGA GTAAGGCAGC TGAGGCACCT TGGGTGCACA ATTTAAGGAA 540
GAGCCTCTCT TGCCTCCCCT AGTCCCTGTC CTGGAAGCTG GGAGAGCTGG TCTCTAGGGG 600
CTCACTGTGG CACCCAAATT GCGGCCCACC CATGGGTGAA CCGGGCTTCC CTATGAACAC 660
TGAGAAGGCC CTTGTGGTTC CCACACACAC TCTGAACACA GGAAGGAAGA GGAGGCATAG 720
ACTCTGGGCC ATGGTGGCCC CAACTGCTCC CTAGTTCACC TTCCCCAGGC TTGTGAAGCC 780
CTGCCACCCC TCCCCAAGCC TGGGTTCCTC CTCTTCCCTC TTCTTCTTCC TCTCCTGCCC 840
TGATTCTATC AGGACCCAAC AGGAAACCTG AACCCCCACC TGGCATCCCT CCCCAGTTCT 900
ACCTTCAAAC CTCTCTCTGA AGGCAGATGC AGGCGCCCTT TAATGACTCT GGCCGATGTA 960
TTCTGTGAGG CCATGAGGGA AATCCTGGGC AGGCCTCATG GCATGCGCTT GTAGGGCCCA 1020
ACGCTGACCA GCACAGAAGC CTACAACCCA AACAAGGCCT TGAACCCCAA ACAACCTCCT 1080
GGAAGAGGGA GCTCTTCACC TGCCCCCACA GCCTTGTCCA CAGAACCCAG ATCCATCTCT 1140
GACAATATCT ACTGTGTGCC AATCCTGTGC CAGGCACTGG GGCCATTATA GATGAGGTGG 1200
TCAGGGCAGC CCATCTTAGG AGGTGACATC TGAAAGGAGG ACTGAATGAT ATGAGGGAGT 1260
GGGCCGGAAG GGAGGGCAGA AGAAACAGTG TGTGCAAAGG CCCTGCAGTG GGCGTGGGCA 1320
GGATAGGAGG AGCGGAGGCA GTGAGGGGGT GGAGGCCAGG ACGGCCACCA AGGAGCTGGG 1380
ATTCCAACTC AGGTTGGTCT GTCATCTGAG CCAAGGACCC CAATTCTCCA GGGAATGGGT 1440
GGGAAAGGGA TTTGCCAATT GATCCCTGCA CTACAGACCA CAAAGCTGCA CCAACTGTGA 1500
AGAAGGGTCA GCCACAGGGG AGGATGTGGC ACAGGTGCTC ATGGGATTCC AGAGCACACC 1560
CTCTCGGCCT GCTAATGGAG GCAGCAGGGT GAGGATGGGT GCCCACCATC CCTCCAGGGA 1620
GCTGGGCTGC ACCCCACCTG CTGTTCTGCT CCCACCAGGC ACTTCCTTGA TCCTCCTAAC 1680
TGGAGTCGGC GGTCCTCGTG TTCTCAGCTG GTCGTGTATC CAGCAGTGGC ACAGGCTGCC 1740
CTTTGTGCAC TCATGGCTGC CCCGGGGGCA CAAGTGTGTG CCAGCTCTTC CCGGAATGGG 1800
ACGCACCCAT GGCTGGAGCC CCAGGTGCAC CTGGGCGCAG GTCCTCTTGA GGAAACTAAG 1860
GCTCAGACGG AGGCCTCGTG CCCAAAGTCC CACAGCTGCC ATATGAAGAA TCTGGTACAC 1920
AAACCCCATT CTGCGGCCCC AGAGCCTGCC CTTCAGCCCC AGCCTGTGGG GGACAGCAGT 1980
GAGCCCCAAC TCCGGCCTGC CTCTGCCCTG ACCAGCTATC CTCATTTGTC GCAGTTCAGT 2040
GAGTGTGTGC AGAGTGCAAA GACAGAGAGG ACAACACGAA GCTCTTTAAG GCTCAGCTCC 2100
GGCACTGCCT CCTCCTGGAG GCTTCCTAAC CACCACCCCC CCAGACCTAT CCACCTGCCC 2160
TGCCAAATTA GAGGCTGGGC CTCAGCTGGG GGCCCCTCCT GTCAGGGCCT GAACCAGCTG 2220
TGACCCCAGC CTCACCCAGC ACAGGGCTGA CCACAGCAGG GACCCCAGTC AGAGGCCGTG 2280
CAGACTCCAG CCATGGCTTC CTCCACCCTC GTCTGCCTCC ACCCCCATCC CCTAACTGGT 2340
GTCTCCCTGG 2350