EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-25076 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr5:149889460-149892420 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUNMA0488.1chr5:149891760-149891773ATGATGATGCCAT+6.01
RREB1MA0073.1chr5:149891798-149891818GTGGTGTGTGTGTTGGGGGG-6.02
RREB1MA0073.1chr5:149891492-149891512GGGGTGTGGCTGGGTGGGGG-7.11
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00311chr5:149889467-149899312Adipose_Nuclei
SE_00977chr5:149886183-149890314Adrenal_Gland
SE_00977chr5:149890383-149892856Adrenal_Gland
SE_01628chr5:149890664-149892339Aorta
SE_02326chr5:149889722-149892651Astrocytes
SE_03211chr5:149889842-149890771Brain_Angular_Gyrus
SE_03211chr5:149890880-149892403Brain_Angular_Gyrus
SE_03966chr5:149889344-149896283Brain_Anterior_Caudate
SE_04872chr5:149875045-149893968Brain_Cingulate_Gyrus
SE_05832chr5:149875010-149907949Brain_Hippocampus_Middle
SE_06896chr5:149889676-149893424Brain_Hippocampus_Middle_150
SE_07847chr5:149889558-149892867Brain_Inferior_Temporal_Lobe
SE_23236chr5:149889236-149892835Colon_Crypt_1
SE_23910chr5:149889310-149892565Colon_Crypt_2
SE_26565chr5:149882831-149893868Esophagus
SE_28046chr5:149887835-149892781Fetal_Intestine
SE_28971chr5:149886325-149892785Fetal_Intestine_Large
SE_31636chr5:149885286-149893974Gastric
SE_33034chr5:149890889-149892048H1
SE_37040chr5:149875517-149899787HSMMtube
SE_40767chr5:149889302-149892638Left_Ventricle
SE_41817chr5:149889322-149890402LNCaP
SE_41817chr5:149890430-149892411LNCaP
SE_42162chr5:149875421-149894184Lung
SE_45685chr5:149889642-149900123Osteoblasts
SE_46674chr5:149890971-149891909Ovary
SE_47292chr5:149889382-149891376Panc1
SE_47574chr5:149889692-149890787Pancreas
SE_47574chr5:149890791-149892382Pancreas
SE_48665chr5:149889694-149892370Right_Atrium
SE_50195chr5:149889274-149892822Sigmoid_Colon
SE_51701chr5:149889652-149892549Skeletal_Muscle_Myoblast
SE_52554chr5:149889187-149892861Small_Intestine
SE_53308chr5:149875512-149896398Spleen
SE_55717chr5:149890766-149892657u87
SE_63488chr5:149889382-149892601HSMM
SE_65479chr5:149885411-149892253Pancreatic_islets
SE_67601chr5:149890766-149892657u87
SE_68965chr5:149890564-149892248H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5149889843149890400
Enhancer Sequence
CTCTGCAGTG CAGGCTTTCC CAGGAGGCTG AAGCTCAGCT AGAGAAGCTG GGTCAGCAGC 60
CCTGGGCCTG GTCACCTCCA GGAAGCCTCT CTCCTGGGCT GCAGACCTGG CTTGGGAGTG 120
GTGTGGAAAG TAGGACTGCA GAAGGGTAAC GAACAGGGGC TGTGGGGTGG GCTGGGAGGG 180
GCATCCTAGC TCCACCTCTG CCCAGCTGTG TGACTTCGAG CGGTTGCTTA CCCTCTCTGA 240
GCCTCCATTT CCTTGTCTGT AAAGTGCTCA TAGCAGTGAC ACCTCTTTCA GGGTGTTAGG 300
ATTGAGCGTG ATGGAGCAGG TAAGGCTCCT GGCACAGCCC CACATGTTCG CAGGAGCTTA 360
ACGTTGGCCG CCAGTAAGGG AGGTTATGAT ATGTGTTGGG ATATGCTGCT TTGTTCCTTT 420
TGAGTGTCTG TGATCTGAGC CTAAGGAAAA AATAGTTCTG GATGGATTTG ACTCTGTCAT 480
AGGCAGATTT GGGGATAGGG TGGGCAGAGA GCCCCATTTT GGGAAGATTT GTGGCCACTG 540
CATAACATTC TGTGTGATGG ACCTGACAGC CTTGGTGTGC GTGAAGAGCC TCAGTGGGAC 600
TGTCAGGACT GTCCCGTCCT TGGGACGGGA GGGTGGCAGG TGACCTGCCG TGTTCCCCAC 660
ACAGCCCCAC CCCCAGGCTG TCTGGTATGT TTGCTCGGTA AGCCCTTTTT TTCAGAGCTG 720
GTACAAAGGT AAACTCGCAA CTCAGGCCCT GTTGGAAGAA GGACACATTC TCAACAAGTG 780
AGGTCTAAGT TCCTGAGGTT TTCTGTTGGG CCTTCCCTGC CAGGGAACCC AGAACAGATT 840
CACAAGTTGA GAACCAGGGA GTGAACCAGT AGTGCTTAAT GCTTTGTTTC CTTGTTGATT 900
GACGGATGAT CTGTGAGCTA CTTCCAAGAA AGATCACTAG AGGCTGCTTG TGATACTAAA 960
ACACATATAA AATGGATGAA AACAAACACA GACAGAAAAC TATTGAAAAG GAATGGAGAA 1020
AGGGATGTGC AGGGCATCTG GCAAATGTTA GCTGTCTTAG GTGATCACAG AGGGGCTGCG 1080
GAGATGGGGG ATGAGGGGCC CAGGCTCTGG AGCCCAGCAG CTGTGTGCTG AAGTTCCCAT 1140
TCACCCCCTT ATTAGCTCTG TGGGCTGCAG CAAGTGACTG GCCTCTTTGG ACCTCAGTTT 1200
CTCATCCGTA TAATGGGGGG AATCTAGGTC ATGGTGCTGT GGTAAGGTTG AAATAATGGC 1260
ATGTAACGCA GACATGGCAT GTCTCATAAA TGGAAGTTAA TGTTATTAAT GCATTTAGCT 1320
TGGAGATGCC GCGTAGCAGA TTCACAGAGG GGAAGGTAAT TGGCAAGGGC ACAAGGCTCT 1380
TGAGTACCTG CTGTGGGTAG GAGATGGCTT GTGCCTTGGA AAGCTTTCAG TGAAGTTGGG 1440
AGCCCCATGT TCTAGTTGCA AGAACAACTG ATACCTGGTG TTGCGTGGTG GGATGTGGAG 1500
CAGGGGAGCT CAATCAGGAC TTTAGAAATC CAGAGCAGGC TTGTTCACCT CCCTGCTGAG 1560
GCTGGCATTG GAGGAGGAGG GACAGGGTTT TAATGGACAA GAAAATGGAC CAAGGTAAAT 1620
GAGAGTGGGG CACACCAGAC GGCACAAGCC AGGAGGTCCT TTCCTCTCTC TGGGTCTCAG 1680
TGTCCCCAGG GGCTTACTGC AGGGTAGACT GTGCTCTCTG TGGCCCTGCG ACTCTGAGCC 1740
AGACCTCCAA CAGTCTCTTT CCCGGTGGTG GTGGTCCTGG ACTCTGGGGT GACTGACAGG 1800
CGGCAGCTTG GCTCCTGGCC AGGCAGCACT GTGGGGGTGA TGGGGGATGG GGCATGTAGC 1860
AGATTCCAGC AGAGGAAGGG ATTTGCTTCT GGTCTCGGCC TCCCAGGGAT GTAATCACGC 1920
TGGAGAAACT CCCGCACAGC TGGGAAGCAA ATGTGGAGGA TTTTCCTTGC TGAGCTGGAT 1980
GTGGTGGGTG GGGCAGGCTG TGGTAGGGTG GCTGGTGGAG CTGGGAAGCT GTGGGGTGTG 2040
GCTGGGTGGG GGTGATGATG TGACTGTGCT GGGGGTGTGA CTGGCTGGGA GGGGCTGGAT 2100
CAGCTATGGG GAGTGGCCCT GGGTGCATGT GGGGCTACCT GTTCCCCAGG CCTGCAGCCA 2160
CTGCTACGCC CTCCCCTGCT CAGGTCCCTG CCCAAGTCCA GGTACCCACC CATTCACATC 2220
CTTCTGAGGT TGCTGGCAGA GCTCTTTCTG CACTGACCTC CTCTCAGCCC CCACCCCATG 2280
TGCATGTGGC CCAGATGCCT ATGATGATGC CATTTGAGCC TGTCATGTGC ATGTGAATGT 2340
GGTGTGTGTG TTGGGGGGGC AGGGAGCAGT GTGTGGTCCA CAGAGGGCAT TGTCAAGAGT 2400
GACCTAGGCT GGAAATAAAA TGTGGGCTGG GTGAGCATTC AAGGCCCTGG GCACCTTCCC 2460
CCATTCACTG CAGCCATGTC GTACCAGAGA CATAAAACCT TGGGTTCCAG AGACCTCTAG 2520
AAACCCTTGT GGAAAGGTCA TGGTCGCCAC TGCATTTTCA GTGCCTAGTG GCATGCTTGG 2580
CACCTAGTGG TGCTCAGTAA ATACAGGATG AGGAAACAGG TCGTTTGCTT GTTCCGCACT 2640
CCCAGAAAGA TCTCGAACCT CCTTCCTGGA TCCCATTCTC TTGCTCCTTC CCTCTGGCGT 2700
CAGCCTGGCC TCCCTTCCTC TCTCTTTCTC AATTCACTAC TAATTTGATA TGTGGCCTTG 2760
GGCCAGTTCC TTCCTGAGCC TCACTTTCCA AATCTGTTAC TGAGTAATCA TTTTATTAGC 2820
TTATATTACC ATGTGCCAGG CACTGAGCTC AGTGTTTTAC ATGCCTCATC TCTCTTTGTC 2880
TTGGTAGCTG CCCTGCAAGA TAGATAAGTA GTATAAACCC CATTTTAGAT TTAGTGAAAC 2940
TGAGGTTCAG AGAGGTTGAG 2960