EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-00231 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr1:8498000-8500610 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs34976449chr18498327hg19
rs301803chr18498680hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELF3MA0640.1chr1:8498713-8498726TTACTTCCGGCTA-6.54
ONECUT1MA0679.1chr1:8498368-8498382AAAAAATCAATATA+6.62
ONECUT2MA0756.1chr1:8498368-8498382AAAAAATCAATATA+6.91
ONECUT3MA0757.1chr1:8498368-8498382AAAAAATCAATATA+7.19
Sox6MA0515.1chr1:8499620-8499630CCATTGTTTT+6.02
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_00045chr1:8497982-8499894Adipose_Nuclei
SE_02022chr1:8498913-8499948Aorta
SE_03947chr1:8498778-8499975Brain_Anterior_Caudate
SE_04978chr1:8498182-8500162Brain_Cingulate_Gyrus
SE_07042chr1:8498385-8500215Brain_Hippocampus_Middle_150
SE_07921chr1:8498882-8500242Brain_Inferior_Temporal_Lobe
SE_11329chr1:8496575-8500743CD20
SE_25808chr1:8497845-8499987Duodenum_Smooth_Muscle
SE_28078chr1:8498322-8500011Fetal_Intestine
SE_29095chr1:8498172-8499988Fetal_Intestine_Large
SE_29887chr1:8497659-8500219Fetal_Muscle
SE_31622chr1:8498048-8498478Gastric
SE_31622chr1:8498521-8499967Gastric
SE_40658chr1:8498953-8499664Left_Ventricle
SE_41679chr1:8499010-8499949LNCaP
SE_41679chr1:8500125-8500471LNCaP
SE_42166chr1:8498911-8499835Lung
SE_48103chr1:8498317-8498850Psoas_Muscle
SE_48103chr1:8498931-8499864Psoas_Muscle
SE_48600chr1:8498898-8499546Right_Atrium
SE_51176chr1:8497978-8500178Skeletal_Muscle
SE_53408chr1:8499004-8499850Spleen
SE_54752chr1:8497250-8500103Stomach_Smooth_Muscle
SE_58576chr1:8455425-8501956Ly1
SE_60225chr1:8480836-8499894Ly4
SE_60758chr1:8454848-8500160DHL6
SE_62661chr1:8450826-8509851Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr184985928498880
Number: 1             
IDChromosomeStartEnd
GH01I008437chr184976518500633
Enhancer Sequence
GAAGGAGAAA CCTCAACAAG TGCTGTTAGA TTTCACTTTT ATTATTATTT ATTATTATTT 60
TTAGAGACAG GGTCTTGCTC TGCCACCTAG GCTACAGTGG TATGATCACA GTTCACTGTA 120
ACGTGGAGCT TCCGGGCTCA AATGATCCTC CTGGCTCGGC CTCCCAAGTA GGTCAGACTA 180
CAGGTATGTG TCAGTTACCA TGCCCAGCTA ATTTTAAAAA TATTTTTTTG TAGAGACGGG 240
GTTCTCACTA TGTTGCCCAG GCTTGGTCTT GAACTCTTGA TTTCAAGCAA TCCTGCTGCC 300
TCAGCCTCCC AAAGAGTTGG GATTATGGCA TGAGCCACTG TGCCCAGCCA GATCTCACTC 360
CTGTAGGAAA AAAATCAATA TAGGATAATT TTCAGTTAAA AAGATGTATA TACATACGAA 420
GAGGGAGACC TACTAAAACA TCTGTTACAA CAGCATATAG TAAGGCAGAA TCTTTGCATT 480
TTCAAAATGT TTTCATAAAC TTTATTTGTT AGAGCAATTT CAGGTTCACA GCAAAACGGA 540
ACAGAAGGTA TAGGGATTTC CCATATAGAT GGGTCTCTGG ATTTTTCAGC TAATTTTGAA 600
AAATAGGGAA AAGAGCAATC AGCATTTTGT GCTCACTACA GTAAACCAGG AACACAGGCA 660
TCAGGAGAGC TGGGCTCTGA TTCAAAGGCC TGATTCTAGC AAGGCCTCAC AGTTTACTTC 720
CGGCTAGCCA TGAACACTCT CTGCGCCTGA GGTTTTCGTG GAAAGACAGC ATCACAAGTA 780
CTCAAATGTA GCGTTTAAAA GTACTAACTT TTAAAATGTT GAATGTTCCA GTAAAACAGT 840
TAAAGAAAAA AAAAGGTAAT AATCCAACTA AGTAAAAATA TTAACTTATA CATATCTGGA 900
TAGATGATAA GCTCATTACA GGCCCTAATT TTATTATTTA AAATGTTTAC AACAAAACTC 960
TCTAATTGAT ATTCTCCCTC TCTCTCTCTT TTTGCCTTGA TATGGTTTCT ATAAACTCTT 1020
GGTTTAAAAA AGAAAAAAGG TCCATTTCTG AGGCTTGGGT TTACTGTACT TACAGTTCCA 1080
CCAGTAAATC GTCTCCCAGT CTGGGCTGGA GAAGCGCTGG CCACGGTTTG ATTGCTCCAG 1140
CCCCAGGTTG CCAGGCAACC CACACAAGGG GGAAGTCTGA GAACCGCTGA CAGATAGCCA 1200
AGTGGCTGAA ACAACAGACT TCTCTCTGTC AAAAATGTGT TTGAGAGAGC CACTTGCCCA 1260
CCTCTGCTCT CTGCTAAACA CTACATGATT GTAAAATCAA AATCAAAAGG CCACTGTAAT 1320
AAAAACACAC TTCCTGCTCA ATTACTAATT GTTCTAAAGC TGTGGGGAGG CCCAGATCCT 1380
ACAGTGTATG GCAACAGAAA TGCGATACTG TAAATGAGAT AAAGCCAGCA GCATGCAAGA 1440
AACCTGATCT AAATGCATCT CCGTAGCTTC AAGTCAGGAG AGCTGGTGTG TGGAGGAATC 1500
AACTGCCTAA GAAAACACCA GGAAGAAAAT AATGAATGTC AAGATGTTAA AGAAACAAAC 1560
CAATCAATAA CTACGAAGCT AGAGGTCAAG ACTACTTAGT AATAAAACCA AGAACATTCT 1620
CCATTGTTTT GAAACACAAT CTGGAGGCAA TGAAAGTTTT CTCCCTCAGA TGGAAAGGAG 1680
GAGCAAGAAA GGTCAATGAC CCTTGGGAAC CACACCCCCT GGCGGTTCCA GGTGGATTCC 1740
CTGATACTTG ACTGTAAATG GGATTACAGG AAATAGTAGC ATCCTTAGGA TAATGCAGGA 1800
CAATAACAGG TCTGAGAGTC TAATGCAACA TTTAAAATAC CTATGGTGTG AGCTGGGCAC 1860
AGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGTGGGTGGA TCACCTGAGG 1920
TCAAAAGTTT GAGACCAGCC TGGCCAACAC AGTGAAACCC CGTCTACACT AAAAATACAA 1980
AAAATTAGCT GGGCATGGTG GCAAACGCCT GTAATCCCAG CTACTGGGGA GGCTGAGGCA 2040
GGAGAATTGC TTCAACCCGG GAGGCAGAGG TTGCAGTGAG CTGAGATCGC GCCATTACAC 2100
TCCAGCCTGG GCAACAAGAG TGAAACTCCC TCTCAAACAA ACAAAAACAA AATATCTATG 2160
GTGCATGTAC CAAGCCAGTA ACATTGTGCC CAACACCAAC TCTATGCAGC ATCCTTCCAT 2220
GAAACCACTG TATTGAAACT GTCATCTTGG ACTCTGGAAA CTATTTGTAG TATGTGGAAG 2280
GGGCCAGCAC TGAGTGCACA GTTCTTTATC TCTTCTGTGC CATGGACCCT TTGGCAGTCT 2340
GGTAAAGCCT GACTCCTTCT AAAAATGGTT TATGGCCAGG CACGGCTCAT GCCTGTAATC 2400
CTAGCACTTT GGGAGGCCGA GGCAGGCGGA CATGAGGTTA GGAGATCGAG ACCATCCTGG 2460
CCAATATGGT GAAACCCTGT CTCTACTAAA AATACAAACA ATTAGCTGGG CGTGGTGGCG 2520
CATGCCTGTA ATCCCAGCTA CTCAGGAGGC TGAGGCAGGA GAATCACTTG AACCAGGGAG 2580
TCAGAGGTCG CAGTAAGCCG AGATCATGCC 2610