EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-16786 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr17:55946560-55948420 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr17:55947863-55947881CCTGCCCTCCTTTTTTCC-6.03
JUNMA0488.1chr17:55946842-55946855ATGACATCACCTT-6.17
ZNF263MA0528.1chr17:55947454-55947475TCCCTCTGCTCCTCCACCCCC-6.16
ZNF263MA0528.1chr17:55947448-55947469TCCCCATCCCTCTGCTCCTCC-7.46
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00907chr17:55944357-55947875Adrenal_Gland
SE_01614chr17:55944134-55947871Aorta
SE_03878chr17:55944437-55946925Brain_Anterior_Caudate
SE_04783chr17:55943537-55956092Brain_Cingulate_Gyrus
SE_06590chr17:55943471-55960413Brain_Hippocampus_Middle
SE_07738chr17:55944499-55948101Brain_Inferior_Temporal_Lobe
SE_25794chr17:55944506-55947191Duodenum_Smooth_Muscle
SE_26551chr17:55944511-55947183Esophagus
SE_26551chr17:55947305-55947875Esophagus
SE_27772chr17:55944963-55947698Fetal_Intestine
SE_28796chr17:55945538-55947248Fetal_Intestine_Large
SE_29569chr17:55944789-55947279Fetal_Muscle
SE_31404chr17:55945048-55947269Gastric
SE_33448chr17:55944917-55948315H2171
SE_34254chr17:55944285-55947872HCT-116
SE_37539chr17:55944891-55948478HSMMtube
SE_38977chr17:55944491-55948134IMR90
SE_40601chr17:55944508-55946769Left_Ventricle
SE_42102chr17:55944456-55947344Lung
SE_44235chr17:55943907-55949134NHDF-Ad
SE_44887chr17:55944695-55948223NHLF
SE_46579chr17:55944902-55948357Osteoblasts
SE_47384chr17:55943677-55947129Panc1
SE_48056chr17:55944315-55947025Psoas_Muscle
SE_50156chr17:55944728-55947943Sigmoid_Colon
SE_51111chr17:55944588-55947054Skeletal_Muscle
SE_52082chr17:55947168-55948059Skeletal_Muscle_Myoblast
SE_52598chr17:55944533-55947403Small_Intestine
SE_54487chr17:55943323-55956053Stomach_Smooth_Muscle
SE_56380chr17:55944455-55948275u87
SE_63290chr17:55922884-55976538NCI-H82
SE_63875chr17:55947123-55948110HSMM
SE_65273chr17:55943779-55948012Pancreatic_islets
SE_67933chr17:55944455-55948275u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr175594712655948047
Number: 1             
IDChromosomeStartEnd
GH17I057866chr175594392855948923
Enhancer Sequence
GGAGACACCT GCTGAAGGCC GGCCACCGTG GCCAGCCATG GCCGCTGTCC CAGCCCTACC 60
CACCCATCTG AGGACAAATG CAAAGAAAGA GCAGGCTTCT TCCCTGGCCA GAAGGGAGTT 120
TAAAGCAAGG AGGATGTGGA GTTCCAGGAG CTCCTCTTTC CCCTTGTGGA CTTTGTTTCC 180
TCCTCTGTAA AAATGGGGAG GGTTCAGCGG TCTACTGTGT GTGCAGACAG CCAGCTCGTG 240
TGTGCTCCCA ACTGTCCACG CCTCTGACCA ACTCCATGTT TCATGACATC ACCTTGGTAG 300
CTTGGGAGTA TTTCCACCAT GGAGGTCACC AAGCACTACA TATCAGGCTC CCGCTGCACC 360
CAGAGTTGGC TGTGAAACAT TCACCAGCAC ACCAGGGGCC TCCTGCACCC CGACATTCAT 420
GTGACAGTCA AATGAGGTGC TGGCTCAGAG CCGGCATTCA CCTGTAGCAA GTCCCTTGTC 480
CTTCCTGCCA GGTAAGCCCA TCCATTGCTC CCTCCCAGCC ACAGGGTTTC TGGCTATTAG 540
ACAATGAGTA GGAATAGAAT GGGACTAGTC CTGGAGTCAG AACCCCACCG GCCACCCAGA 600
GTCTCCCGGG CTCGCTCAGC ATCCACTTGG GTTTTTTGCT GGTTTCTGAA GCCCCTGCTC 660
TCTGTCCTGC AACTTGGTTA ATCCCCAGTC ACCTTGCCTG CTAAGTCCCC TTTGAGTCAT 720
TCTGATCCAT CTCAGCAGCC CCGGTATCTC TAGTTAATTC AGGATCAAGG ACAAGAGGCT 780
CCTGCTTAAA ACTCCCAGCT GCACATCTGC TGAGCCCTAA GCTCCCAGCC TGCTGCTTAT 840
GAGTCAGTTC CACAGGATTT TCTCCCTTCA AGCTGGGATC AGCTCAGCTC CCCATCCCTC 900
TGCTCCTCCA CCCCCAACTC CACTGCATGA TGCAAGGTCT ATTCCAGGCA AGAGCCCTTC 960
TCCGAGGTGG GCAGCTTGTG TACATGTGGG GCAGGGGGCA CTGACTGATG AGGGGCCACT 1020
GTTCGCACAC AGGCACCAGG TCATCGTTCC CAGCTGTGGC TCAACCCAGT AGTCTGCGCA 1080
TCCCAGGAGC ACTGCAGCCC CCTCACCCCT ATCCAACCCT CTTTCAGCCA TCAGAGCTTC 1140
TGAGCAGAAG GGCCTGGCCC TCTTTACAGG CAATTCTTAC TTCCCACCAC CTTGTACACA 1200
AAGCTAGAAA TTCCTCTTCC TCCAACACCT AGGGCAAGGC CCAACAGATG GCAGATATTC 1260
TCCAGCTATG TCATGAATGA ATGAGTAAAC TCCCCAGATT AATCCTGCCC TCCTTTTTTC 1320
CCATGCATTT GCTAAAATCA GTAAGTCCTC AGCTTTGCTA GTTTGTTCTA CCTGTTTTCT 1380
GGGCATTTCT CCTTACAAGA CCATAAGCTT CCCCAGGACA CAGACCAAGA CTTATGAGTC 1440
TCTGAGCCCC ACCACGGGGC ATTTTGGGGT CCTTTTCTTC TTTTTTTTTT TTTTGGAGAC 1500
AGGGTCTCAC TCTGTCACTC AAGCTGGAGT GCAGTGGCAT AATCACAGCT CACTGCAGCC 1560
TCAACCTCCT GGGCTCAAGT GATCCTCCCA CCTCAGCCTC CTGAGTAGCT GGGACTAGAA 1620
GCACAGGCCA ATATGCCCAG CTAATTTTTA GTACTTTTTT GGTAGAGATA GGGGGGTCTC 1680
ATTTTGTTGC CCAGGCTGGT CTTGAACTCT TGGGCTGAAG CAATCCACTC TCCTCGGCCT 1740
CTCAAAGTGT TGGGATTATA GGCGTGAGCC ACCGCACCTG GCCATGTGTC ATTGACTAGC 1800
CTACACTCGA GGCATAGGTT GAGAGTTCAG CCAGCCTATG TTACTTGAAC ACAACTGTGG 1860