EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-12437 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr17:27480970-27484650 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr17:27482491-27482509GGGAGGGAGGGAGGAAGT+6.29
NR2C2MA0504.1chr17:27482564-27482579CGGGGGCAAAGGGCA+6.54
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_03450chr17:27480460-27484485Brain_Angular_Gyrus
SE_03910chr17:27480341-27484877Brain_Anterior_Caudate
SE_04884chr17:27475155-27487900Brain_Cingulate_Gyrus
SE_05843chr17:27474727-27488125Brain_Hippocampus_Middle
SE_07476chr17:27480023-27487637Brain_Hippocampus_Middle_150
SE_07806chr17:27479971-27488254Brain_Inferior_Temporal_Lobe
SE_08959chr17:27481799-27482199Brain_Mid_Frontal_Lobe
SE_08959chr17:27482931-27483429Brain_Mid_Frontal_Lobe
SE_08959chr17:27483861-27484542Brain_Mid_Frontal_Lobe
SE_09987chr17:27480834-27483584CD14
SE_19008chr17:27480940-27483656CD4p_CD25-_Il17-_PMAstim_Th
SE_19489chr17:27480816-27483655CD4p_CD25-_Il17p_PMAstim_Th17
SE_28031chr17:27480548-27484527Fetal_Intestine
SE_28952chr17:27480565-27484674Fetal_Intestine_Large
SE_30293chr17:27482624-27483845Fetal_Muscle
SE_32448chr17:27481182-27484607Gastric
SE_33834chr17:27476050-27486414HCC1954
SE_34898chr17:27480281-27487189HeLa
SE_40250chr17:27481492-27483279K562
SE_41080chr17:27481161-27484677Left_Ventricle
SE_42354chr17:27480302-27484734Lung
SE_47275chr17:27471944-27488173Panc1
SE_49086chr17:27481013-27484627Right_Atrium
SE_50708chr17:27480542-27484757Sigmoid_Colon
SE_51291chr17:27481312-27484287Skeletal_Muscle
SE_52472chr17:27480528-27488119Small_Intestine
SE_53778chr17:27480424-27487753Spleen
SE_65361chr17:27480507-27484732Pancreatic_islets
SE_66834chr17:27481366-27483585Jurkat
SE_68762chr17:27481424-27484531H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr172748154627483618
Number: 1             
IDChromosomeStartEnd
GH17I029153chr172748039827488021
Enhancer Sequence
AGGAAAACTG ATTCCCCTAC CCCAGAGACA AAGTCCTCTG GTGCGAAGCC AGCTGCTTTC 60
CTCTGGACAG AGAAGGTAAG GGCTAGAAGC AAATGGCAGA AATTGGAGGG GTCTGGGAGA 120
AAAGGACAAC CCACTCTAAA TTCTGCAGAG TGTGTGTGTG TGTGTGTGTG CGCGCGCGTG 180
CGTGTGTATG TGGCGCCTAG GCCATTCCTA AGCTGGGTGT CCTGCCACAG AACCCAGTTC 240
TGTGGTTCTC TTCCCCAGGT CGAAGTTAGG TGATGATGGA TGGAGGCAAG AGTGATCAGG 300
CAGCCCTGGG AGAGGCGTGT AGACAGGCCT CAGTGTGCCC GCACAGGGTG GCTCACCTCC 360
CTCGAGGGAG GGCAAGGGCA TTTGGGGTGA GGTGGTCAGG CTGGTACCCC TAGGAGAAGG 420
CTTCATTCCT GCCTGCCCCT CACCTCATCT AAGCAAGAAA CCCCTTTTCT TGTTCAGAAA 480
TCCTGAGGCC AGAATCTCAG GCTGCCAGGG CAATCGGGGC TCTGCCAGGC AAAGCCAAGT 540
GCTAAGGGGA ATAGGGATGT TTGCTGGTCA CCGATTCCAG GAAGACAGGC CACAGCAGTC 600
CCCCCAGGCT TCTCAGGCAG GGGGCCCAGT TTCCCTCTTG CCTCTGTTGA TCTTGAGGCA 660
TGGCCAAGTG AGTGGGGACT CGACCCAGCC TGTGCCCGTG TCCTTTAGGG AACATAGGTG 720
CCTGCTGAGA GGAGGCAGGG CTGTGCCAGG CTCAGCACAT GCTGGGTTCC CCCCATGCCT 780
GAAGTGCCAG GCACACTAGC TCCCACAGCC TGGACAGCTC TGGGGAGGGC GAGGCAGAAG 840
ATGCCAGCCC AGCCGGGGAG GAAATCTTTT ACTGCTCTGA GCCCAGTGCT TCTGCAATCA 900
GCTCCACAAC CAAAGCAGTC CACACATGAG GGAGGGGCAG GGGCATGAGG GAAGGGCCCC 960
CAGCAGGAAG AACTAACCAC ACAAGGAGAT GGTATCAGAC CCTTCCCCTC GCCATGTCCC 1020
TGGAAGGTTC TACTGGAATC TCTAGATACT TTCCCCTTGA TGTGTTGGGG CCGGGCATGA 1080
AACTGGGTGT CACGGAGAGT CATGACAGTC TCACGCTGCC TGACGGTGCT GTCACTGCCT 1140
GGCCTCTAGC CCATGCCACC CAGGGCTGAG ATAGATCTTC CTGCACACGT CTTCTGTCCT 1200
TGCAGAAGCA CAGGCTCCAT CATCACAGGG TGCTATCTTC AGCCTTTCTT CTCCACAGAA 1260
CCAGGCTCAG GGGCTGACAG GGAGCAGTGT TCATCAAGGT GTCCTGACGT CCCACCCTGA 1320
TTGCAACAAG GCTCTGGGGA CATCCACATC TGGCCTTTCC TACAGCACAG AGCTCTGCCT 1380
CCTCCCCACC ACACATGCAG CCCTCTTCTG CCCCAGGGCC GGGGCAGCCT CAGTCCTGCT 1440
GCCAGAGAAG AGCTCCATGG GAAGAACCTG CCGCCCTGTG TGGACCCTGC TTGCCCCAGG 1500
GCCTGGCAGT GAGAGGTGCT GGGGAGGGAG GGAGGAAGTG AGTCAGCTCC CTGCAGAAAT 1560
CTGAGTGGGA GGGAGGAGCC AGCAGAAATG AGATCGGGGG CAAAGGGCAC AGGAGCCAGA 1620
AAGGTCACTA AGAGAGGGAA CCAGGCCCCG AAGGTGTTGC GGGACCCACA GAGTACAAGA 1680
CAGATACAGG TGATGAATTC GGCAGGGCCA CCTCCAACCG AGGCTGGGTG GCCCCAGTAG 1740
GCCAGAGAAC CTGGGTCCAG AGGCCTGGCC CCACCTGAGG ATGGAATCCG AGGCGGCTCC 1800
CCTCCCTGAC TCATGTTCAC ACCAGAGGTA GCAAGGCCTT GTGGGACATG GCCAGCCTCA 1860
TTCTCTCCTC AGAGATGGAG TCTCTGGGCT CCAAGGCCTC CCACTCCCTC TCCTGAGCCC 1920
TACAGCTCCA GAAGCCCAGG TTCCCCATGA CCTGGCCTAG TAGGGACATG CTAAGGTCCT 1980
ACAGACAAGT CACCTAGGCC AGTCAGAGCG GGAAGGTTCC AGGAACCAAA ACTGTCTCCC 2040
AGAGGGGATG GGAGCTGAGC CTGGGCCCCA GGAGCAGAGC AACTGGGGCT GCCTTAGCAC 2100
CCACTCTCTC CTCCCTGGTA GGGACATGTG GGAGCTGTCC CCAGGCTCCA GCTGGAATCC 2160
ATTGCTGTGA CTGGGTAAGA TCCTTGCTGT GAAAATTCCC ATCCTGCTGA CATTCCAGTA 2220
TGAAGGCAGT TCAGGGAGAG CAGCGGAAGG GAAGAGGAAG CCCCACTGGG CCACATTCCA 2280
GCCCCTCAGA GACCTACAGC CAGTGAGACA GGCGCATTCC TCCAAGGTCT GAGACAGACA 2340
CTGCGTAGCC CCCATGTAAT CCTGAATCTT CTTCTCACCC AAGCCTGGCA CCTTCATGTG 2400
GGCTCCTGTG TGGGGGCAGG AGGCAGCCTG TCCCCAGGAC CTCCCTTCCC AGGCTCCTGC 2460
TCCTGGATGC CCACAGAGCT GCCTCTCCTC CAGTCCTGTG AGAGATGCCA GGCCCCAGGC 2520
ATGCAAGAAA CAGTCCATGG GTGGAGATGG GACACGCTAA GGTCCTAGAG ACAAGTCACC 2580
AAGGTCAGTT AGAGCAGGAG GGGTCCAGGA CCCAAAACTG AGCTAAAGTT TTGGTTCTGG 2640
TCTGGAAGAC CGAACAGAGA GAATGAGAAA CCAGTTCCTG AGTACAGAAC CATCTCTTTC 2700
CTTCAACAAA TATCCCCTGC CCTCATGCAG TGCTCCAGCA CTGGAGAAGG AATGAGATAA 2760
CTCAGTAATT ACCATCTTGT GAATGCTATG AGAAGGCTGG GGTGTTGCCA GGTGGGGACC 2820
TGACATGGTC TGGGAGGATC AGGGACAAGT GATATTCAAA CTGAAGCCAA TGTGTAGAAG 2880
TGTACAAGGG AGGGCAGGGA AAGGGGCTAC AGACAAAAGG AACAGCAGGA GCTCAAGGGT 2940
AGACGCCAGT GAGAAGCCTG CATTGCCCCC ACCACTGCTA GGCCCTCTGC CAGGCTGTGC 3000
TCCGCCACTG TTTTTCCACA ACACACAGAG GAAACAACAG CGTGGCCCTG AGCAACACGG 3060
CGAGCCCACT CTTGGTCAGA GGTGACACTG CAGGGATCCT GTCACCCCAA GTGCTATGGA 3120
GATCAGCACT AGCATGCCAG TATGGGCCAA AAAGGTGAGA GGGGCAACGT CCCAGACTCC 3180
CAGATCTAGC ATATGGCCCT CCACTCCTGG GGACCACATC AAATGCTGCC AATGTAGGTG 3240
CCACTTCTCT TCTTAAGGCG TCCCTCTTCC ACCCTTCCCT CTCCCGGCTC CCACAAGATT 3300
GAATCCTGCC TGCTGCCACT TGGGCTCACT TCCTCTGGCT AACCCTCAGG AGACACTGAG 3360
AGCAATGGTC ACACCCTTCT GCAGCACACC ACCACAGCTC AAGAGTGGCC CATCACTCCT 3420
GGTTTCCTTC TGGAAGGATG ACAAGGAGGT GAAGAGGCTT TTAGTGACAG GGCAGCAGGA 3480
GTCAGAAGGT CTGAGCTAGG CAGTGGATTT ATATGGATAT CCGGATACTG CCTTGCTCTC 3540
CCCTATACAG CAGACTAGTC AAGAGCTGAT GGCCTGAGTT CAAGTCCTGG TGAGTCACTT 3600
AATACCTGTG CAACCTTACA CAATTTGCCT AACTTTAACC TCTCAGTAAT GCAGTTTCCT 3660
CACTTTAAAA CAGATTGTTA 3680