EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS037-06868 
Organism
Homo sapiens 
Tissue/cell
ESC 
Coordinate
chr11:75051700-75053250 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:75051998-75052016CCTTCCTGCCTTCCTTGG-6.9
EWSR1-FLI1MA0149.1chr11:75051994-75052012CTTCCCTTCCTGCCTTCC-7.02
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00135chr11:75043906-75064147Adipose_Nuclei
SE_04031chr11:75048090-75054947Brain_Anterior_Caudate
SE_04951chr11:75048891-75064200Brain_Cingulate_Gyrus
SE_05927chr11:75046856-75064439Brain_Hippocampus_Middle
SE_07122chr11:75047688-75064272Brain_Hippocampus_Middle_150
SE_07907chr11:75048701-75062762Brain_Inferior_Temporal_Lobe
SE_09621chr11:75043963-75064807CD14
SE_13044chr11:75052236-75053580CD34_Primary_RO01480
SE_13386chr11:75044177-75055601CD34_Primary_RO01536
SE_14290chr11:75048993-75052021CD34_Primary_RO01549
SE_23271chr11:75049892-75052298Colon_Crypt_1
SE_23271chr11:75052406-75054954Colon_Crypt_1
SE_24003chr11:75049934-75052229Colon_Crypt_2
SE_24003chr11:75052429-75054936Colon_Crypt_2
SE_25192chr11:75049919-75052271Colon_Crypt_3
SE_25192chr11:75052391-75054969Colon_Crypt_3
SE_25898chr11:75044092-75062820Duodenum_Smooth_Muscle
SE_26962chr11:75048304-75052360Esophagus
SE_26962chr11:75052365-75054928Esophagus
SE_28109chr11:75049709-75056802Fetal_Intestine
SE_29208chr11:75047729-75056855Fetal_Intestine_Large
SE_31429chr11:75048137-75054991Gastric
SE_41608chr11:75050385-75052279LNCaP
SE_41608chr11:75052412-75054771LNCaP
SE_42220chr11:75048188-75064405Lung
SE_46889chr11:75049941-75052220Ovary
SE_46889chr11:75052538-75053369Ovary
SE_47208chr11:75043719-75064671Panc1
SE_49380chr11:75048356-75052354Right_Atrium
SE_49380chr11:75052362-75054960Right_Atrium
SE_49998chr11:75046773-75051856RPMI-8402
SE_49998chr11:75051883-75052281RPMI-8402
SE_49998chr11:75052387-75054874RPMI-8402
SE_50175chr11:75048167-75055001Sigmoid_Colon
SE_52494chr11:75048015-75055001Small_Intestine
SE_53599chr11:75048063-75059815Spleen
SE_54712chr11:75043970-75064153Stomach_Smooth_Muscle
SE_59773chr11:75038940-75077709Ly4
SE_65484chr11:75049984-75054384Pancreatic_islets
SE_69190chr11:75050639-75052318H9
SE_69190chr11:75052444-75054531H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr117505176175052000
Enhancer Sequence
CCTACTTGGG GTTGGGAACC AGGAAAGCTG TTGTTTTCTG AGTGTGTGAA ACAGTGGCCT 60
GCTGGCTCCC TTGGCAGAAA GCCAGGCTCG GGGCTCTGCA CAGGGGTGAG GGTTAAGAAA 120
GAGGAGCCTG GGGCCAGGAT GCCAAGGGAC TTCCCTCCAC AACCGCCCCC AGCTTCCTGC 180
TCCCCAATCT CTCCCCACTT CCTCCTAGAG AATCTGCCGT GGGTGAGGGG CCAGAGGGGA 240
GTGGCGCCAG CAGCCCCAGC ACCACACTGC TGCTGCTGGC CCTGGGCAAT CTCACTTCCC 300
TTCCTGCCTT CCTTGGAGCT TCTCCGCTGG CCGGCACAGC CCCCACTCCC TGTGCCCCCA 360
CCCCCGCGCA CTCAGCTGTG TACACTACCC TGGACCATGG AAAAGAGGGA TGAAAGAGGA 420
GGAAGGGGAC ATGGGAGAGG GAAGGAGCTG AGATCCACCC TCAGTCTTGA ATGATGATGG 480
CTTTTTTGTT GTTGTTGTTG AGACAGAGTC TCACTCTGTC ACTCAGGCTG GAGTACAATA 540
GTAAGATCTC AGCTCACTGC AACCTTCACC TCCCGGGTCC AAGCAATCCT CCCACCTCAG 600
CCTCCCTGGT AGCTGGGATT ACAGGTGTGT GCCACCACAC CTGGCTAATT TTTGTATTTT 660
TAGTAGAGAC GAGGTTTCAC CATGTTGGCC AGGCTGGTTT CGAACTCGTG ACCTCAGGTC 720
ATCTGCCCAC CTCAGCCTCC CAAGAGGCTG GGATTACAGG CGTCAGCCAC CATGCCTGGC 780
CGACAATGGC TTTTTATGAA GCCCTTACCC TCTCTGCCCA CAGAAACCCC ATTAATATTA 840
TTATACCTAT TTCCCAAAGG AGAAAACTGA GGCCGGAGAG TTTAAGACCC AAGCTGAAGG 900
TCATGGAGCT AGCAAGTGAG CAGTAGAGCA GAGTCTGCCT AACTCTGAAT TCCAAACTCC 960
AAACCTCCTG CCTCTAGCTC TGGGAGCCCC TCCTCCACAC TCTCTGAGGG TGCTACTTGG 1020
GCAATTCCTA CACAGATGGA AATGACACTG CCCAGCCCTG GGGAGGGAGC CCTCGGCCTT 1080
AAAGAGTCCC TCGCTGAGGA CTAGTTTGGG AACCACAGGA CAGTCCCAAA GACAGGACCA 1140
AGGCTCAAGG GCAGGACATG CTTGGGGAGC CAGGTGGGCA GACTGCTGCT CCCAACTGTC 1200
TTCCCTTCCC ACCCAGTCTA GGCTGGCTCA GACTCCTACA CTGTCTGCCA CTTCCAGAAG 1260
GCAGGGCTGC CAGAGGCCAA GCTGTCCCGC CAGAATCACA CTGCTGCTCA CGCCCTCTCC 1320
CCTCCTAACG AGAGAAGGAA AGGGTCCTAG GGAGGAGCCT CTAGGCCAAA GCCTCTCCTA 1380
CTTCCTGCTT GACACATAGA GAAACTGAGG CCCAATGAGG AAAAGCAGCT TGCCTATGGC 1440
AGCACAGGGA CAGTGAAGAA GTGAGATCCC TGTCTCCCAG GCCAGAGCCC CTTCCCTCCA 1500
TTCACCCCAC TTGGGTGCTC TCCTCAGATG GCACCTTTGG GCATCTGCCC 1550