EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-06172 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr11:64654790-64657330 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr11:64655525-64655544GGGCGCCCCCTAGTGGTGG-7.54
HES2MA0616.2chr11:64657276-64657286GGCACGTGCC+6.02
HES2MA0616.2chr11:64657276-64657286GGCACGTGCC-6.02
KLF16MA0741.1chr11:64656118-64656129GGGGGCGGGGC-6.02
KLF5MA0599.1chr11:64655497-64655507GCCCCGCCCC+6.02
KLF5MA0599.1chr11:64656119-64656129GGGGCGGGGC-6.02
SP3MA0746.2chr11:64656117-64656130GGGGGGCGGGGCG-6.11
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00271chr11:64654337-64656075Adipose_Nuclei
SE_04490chr11:64654855-64655854Brain_Anterior_Caudate
SE_05656chr11:64654701-64656234Brain_Cingulate_Gyrus
SE_09896chr11:64654766-64656187CD14
SE_10358chr11:64655436-64656182CD19_Primary
SE_12689chr11:64656102-64656404CD34_adult
SE_20122chr11:64654945-64656122CD56
SE_20852chr11:64654657-64657583CD8_Memory_7pool
SE_26639chr11:64654879-64655990Esophagus
SE_27915chr11:64654364-64662641Fetal_Intestine
SE_28833chr11:64654274-64662702Fetal_Intestine_Large
SE_34934chr11:64654761-64656076HeLa
SE_40087chr11:64654762-64657486K562
SE_42214chr11:64654918-64656159Lung
SE_47340chr11:64654644-64655914Panc1
SE_48135chr11:64654749-64655760Psoas_Muscle
SE_50675chr11:64654606-64662582Sigmoid_Colon
SE_52636chr11:64654615-64662672Small_Intestine
SE_53384chr11:64654692-64656139Spleen
SE_54661chr11:64654478-64655775Stomach_Smooth_Muscle
SE_57005chr11:64654805-64655546VACO_400
SE_57005chr11:64655583-64657169VACO_400
SE_58521chr11:64614515-64656437Ly1
SE_59680chr11:64615469-64656889Ly4
SE_61730chr11:64614382-64656411Toledo
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116465479164657200
chr116465622164657000
Number: 1             
IDChromosomeStartEnd
GH11I064886chr116465439764662615
Enhancer Sequence
ACCCAGCTGT CCTTTATTAG GCACACCATG TGGCCTGGTC CAGTGTTAGG TCCACCACTC 60
CATGACCTGA CAGCCCCTGC TGGAGAAGCA CCCTGCAGTA GAATCTGTGC ATTACAATAC 120
TCATTATAAT CCCAACAGTG CTCATAATAA CAGCGCTCAT AATAACCCCA AGTGTTCTCT 180
TCACTATACA GCAGTGAACA AGAGTGAAGA AGCTTCGGCT CCATCAACTG CATGAGACTC 240
AGCCAGACAC GGCACCGTGA TTCCATTTAC ATTAATAACA AGAAAGCCAG ACAAAATGCT 300
CGCAGACTGT TTGGGAAAGT GTACGGGGTA GTAAATCCCA GAGAAAGGAG AGGAAGTGAT 360
TACCTTAACA CTCAGAACTG TGCTGACCAT GGGCGGGGGG GACCTGGAAG GGCATATTTG 420
GGGGCTCTGC AGGTTGTTAC ATGGGGACTC ATTGTGAATT CTATGAATAT ACATTATACA 480
GTGATGTTTT ATACACACCA CAGCGGGAAG AGCCCCACCA GGGCCACCTT GGGTAAGGCA 540
GTGCGCGCCT GGGACCCGCA ACTGTGTGTA GGACGCTGGC ACCTGGGCTG TGCCCTAGGC 600
CCAGGACAGT GTCCTGGCCA GGCCAGGCGC AGTTCTAGGC GGCCCGGGGA AGGCGAACCC 660
AGGGGCTGCT CCCCCAGGCC TTGGGAGCCG CGCGGTGGGG AGGGTTGGCC CCGCCCCGCT 720
TGGGAGGGGT GCCCGGGGCG CCCCCTAGTG GTGGCCACCG GGAGTAAGCC TTGCAGAAGA 780
GGAAGCTGTC CCCGCCCGCC CCGCGCCTCC GTCCGGTTTC TGCATCTTTG CCCCTGGCAT 840
TCCTTCCTCC TCCAGTGATC ACGACCTGTT TCTGGGGTTC ACCTCAGCAA ACGCCGACCT 900
CACACTCACC TCTCCCAGGG AGGCTTTACT CCTCCCCGCC TGGGCCTTCT CTCTCTGAGG 960
CTGGCGTACG GTCAATCTGC ACAACCTCTC AGGGCCTCTG TCAGCGTAGC GTTTCACACA 1020
CGTGTGGTGT GGACGATGGG ACAAAGACAA TACTACTGAG GCCTCCCACC GCCAGCTCTG 1080
TGCTGACCGC CCCACTGTGT CTAGGCTCCC TCCCTAAGCA ACTTTGCTCA TGCACAAGGT 1140
CAGTCCTTCT GTGTGCATTT ATTAAGTGCC TCCTTTGAGT CTGAGGCTAC AGGAAAAAAG 1200
TCAGTGGCCG CCACTCCTGG GGGCTTTCAG GCTGGTGGGG GAAATAGCCC GGTGTGGGTG 1260
ATGGGGCATG ATGGGGGCGC TAACATCCCA GCCACAGAGC ATCCAGGGAG CCAGTGAGTG 1320
GGGTAATGGG GGGCGGGGCG GGGGGCCAGG CAGGTGTCCG CGAGGGAGTG ACCCTTGGGC 1380
AGGTCTTGAG GAGTTCTGAG AGGGGTTGGA GGTGAGACCC AGGCCAGGGA AATGTGCATG 1440
GGCCCAGGGC CTGCTGGGTA AAGGACACAG GTCAGTGGGC TCAAGGAGCT GGGGGAGGGT 1500
GCTGGATCCG CCTTGCTCAT GCATTGGAAC AGGTCTCCAA TAGCCCTCGC AGGCCTTTGT 1560
GGGATCGCAG TGCTCTGCAG AGGCAGATGC AGGAGGACCC CCAGGGCAGG GTGGCTGCTG 1620
TCTGCTCCCC TTTCACCCTA TGCCAGTGCT CTGAGTCTGA GGCCTGACAG CCCCAAGAGG 1680
GTTAGAGTCC AGGGCCCTAC CATCCAGCCC ATGTATCCTG AACACCTACT ATGCTGGTGG 1740
GTGGGGGAAG CAGCCAGGGA GGATGAGTAA GTCATGGACC TTGCCCTCAA GGAGTCTGAA 1800
ACTAGCACAG GATTAGATAA GCACACAGGG CTCCTTAACT CTGTAGGGAA TGAGATAAGG 1860
GTGGCGGGAG AGGCCCACGA AGCCGGGGTG TGGGCAGAGA GGGGAGCAGC GCCTGCAGAG 1920
TCATGGGATG GTCTGCAGGG AGGGGTTGCT GAGCTGGGCC ACGGCAGGGG CCAATCGGGG 1980
CCCAGGGATT CAGAGCAGCC AGGACAGTGT GAGCAGAGCT GCCTGTGGGA AGGGGAGAGA 2040
GACAGTGTCT TAGGGGCCAG ATGTTTGTTG GCTGCCTACA GTCCCCAGGA GAAGGTCCAA 2100
CTTGCTCTGT GACTTCAGCA AATGTGCACC CTCTCTGAGC CTGTGTCCTC CTGTCCCAAA 2160
CAGGTTCATG ATGGATGCCA GGAGGACCAG GTCCTGGATG TGCGTGCCCA GCAGACAGAA 2220
AGGGCTCAAT AGCCAACGCC TGTTATTAAG CAATTTGACA TTTATTCCTA GGTCTCTATT 2280
TCCCATTTTA CAAATTTTAT TTTGTAGTAC CAGAAACCTT TTTATTCAAA TGAAAAATTC 2340
TGACAGGGCA CAGTGGCTCA TGCCTGTAAT CCCAGCAGTT TGGGGGGCTG AGGCAGGACT 2400
GCTTGAGGCC AGGAATTTGA GACCAGCCTG GGCAACATGG TGAAACCCCA TCTCTACGAA 2460
AAATACAAAA ATTAACCAGG CATGGTGGCA CGTGCCTGTA GTCACAGCTA TTTGGGAGGC 2520
TGAGATGGGA GGACTGTGTG 2540