EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-10180 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr15:65187750-65190760 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1522744chr1565187874hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gfi1bMA0483.1chr15:65189903-65189914AGCTGTGATTT-6.14
IRF8MA0652.1chr15:65188072-65188086CAGAAACCGAAACC+6.25
NEUROG1MA0623.2chr15:65189741-65189751GACATATGTC+6.02
NEUROG1MA0623.2chr15:65189741-65189751GACATATGTC-6.02
RELMA0101.1chr15:65187966-65187976GGGGATTTCC+6.02
SP8MA0747.1chr15:65189587-65189599AGGGGGCGTGGG-6.04
ZNF263MA0528.1chr15:65188015-65188036GGAGGAGGGGAAGTGTGGAGG+6.14
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00179chr15:65184020-65192302Adipose_Nuclei
SE_00949chr15:65185012-65191657Adrenal_Gland
SE_04179chr15:65187057-65188824Brain_Anterior_Caudate
SE_06037chr15:65183266-65190782Brain_Hippocampus_Middle
SE_07417chr15:65183823-65188537Brain_Hippocampus_Middle_150
SE_09222chr15:65182907-65191234CD14
SE_12439chr15:65183446-65188936CD3
SE_13731chr15:65184779-65190340CD34_Primary_RO01536
SE_19509chr15:65183157-65189177CD4p_CD25-_Il17p_PMAstim_Th17
SE_20451chr15:65183543-65189374CD56
SE_25922chr15:65183499-65191039Duodenum_Smooth_Muscle
SE_26878chr15:65183325-65190494Esophagus
SE_29936chr15:65184729-65188809Fetal_Muscle
SE_29936chr15:65188904-65190496Fetal_Muscle
SE_31256chr15:65183577-65189571Fetal_Thymus
SE_31256chr15:65189614-65190277Fetal_Thymus
SE_31840chr15:65184688-65191003Gastric
SE_42313chr15:65183256-65191830Lung
SE_43954chr15:65183041-65189653MM1S
SE_50230chr15:65183230-65191055Sigmoid_Colon
SE_52555chr15:65183178-65191028Small_Intestine
SE_53569chr15:65182985-65192126Spleen
SE_55484chr15:65183811-65189118Thymus
SE_59387chr15:65156174-65198203Ly3
SE_62974chr15:65169474-65198305Tonsil
SE_67436chr15:65183041-65189653MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr156518946665189943
Number: 1             
IDChromosomeStartEnd
GH15I064891chr156518320165190998
Enhancer Sequence
CTGTCTGAAA AGTGTGCTAA TAAATATGCA AATTTTGGTG ACTTGAGAGG ACTGGTGTCC 60
TCTTGAGTTG TACAGGGCAC AATTTGCAGA TTTGTGAGTG ATCACCAAGC CCCGAAGATG 120
CAGCGAGGTC TCTGGCAACT CCCTTTCTCA GTCCCTTCTC TATTCCTCTC TTCTTCTTTG 180
TCCCTCTCAG ACTGGGACTG GGGGTGGGGG CAGGGGGGGG ATTTCCTACT AGGGTGGGAG 240
GAAGAAGGGT GAAGGAAGTA GGGTAGGAGG AGGGGAAGTG TGGAGGACAA CAGAGGGAAA 300
GGGTAGAACT TATTTCTGCT GTCAGAAACC GAAACCAAAA GTCCTGGCAG GAGTTAATGT 360
GAGAGGGAGG TCTGTAGCAA GAGGCTGAGG AGCAAAGCCT TCACATCTGA GGACAGCAGC 420
CCTGTCAGAG ACACCCTGGC TGCAACCTCG GTGTCACTTA GACCAGGGCT TGCCTCTCAT 480
GCTGACAAGA AGCATGCAAA GGCAGTCTGT TTTCTCTGGG GATACCAAAG GCCCCTCCAG 540
ACCTTACAGT GCCCAGCACT GGTGTTAGGA TCACTGCTGG AAAGGGGAGG GGGCACTAAC 600
TCAAGTCACC ATGTCATCTA ATAGCCCAAG AGTGGGTGAC CCTTTGTCTT GTCTGGTATT 660
AGTCTGTGTG GACCTGCATA CACCCATGAG GCTGAGGCTG GGGGCAGCCG GCATCTGTGT 720
GTCTAGCATA ATGGGGATCC TCTTTCCCCA AGTCAAGCTT AGGACGTGTG GTATAACATA 780
GATTTTTGTG ATCCACCTGG CTGTGAGAGG TCATTTAGGT GCCACAATAA TGGATTCTTT 840
GGGGCACTTC ATACTCTATT ATAACAATAG GAGAAAATGT TTGCAACTTG GACTTGTCTT 900
TTAAAATTCA GATTGTGTGG CCACTATTTC TTGTGAACTT TGTGATTCAA CGAGCCAATT 960
GTGTACTGGG AACCCAGATG GTGCCCCTCC CTTGAGGCTT GCTGGGTCCT CTGTGTAGGG 1020
ATAGACTCTG TTCCGGGCGC CGTGGCTCCC AGTTCCAGAC TGGCAGCCCT TTGAGCGGCT 1080
GAAACTTTAA TTCATCTTTG TATCTCCCAT GATGATAGGA ACCTCCTGTC TCCTCAGGGG 1140
TTCTCAGAGT GTGAGTTTCT GGCTTCTCCA TTCATCCCTC TGAGGCTGAC ATATCTGTGC 1200
TGGCTTCACA GAGGCAGAGA AGAATGGGGA GCATGCAGGG GAGGTGGACT GATGGATCAG 1260
GGCACAGGGG AACCTGGCTC CACCATTTCC CAGCCCTGAG GCCTTGGACA AGTTACATTT 1320
CTGAGTCTCA GTTTCTTCAT CTGTAAATGG GGATGATTTA AATAGTTGAC TTTTACTGAG 1380
CATGTTCTCT GGGTCAGGCA CTGCGTTAAG CATATTGCAG GCAGACTTAT TCAGAAAGCA 1440
TTTATGAGGG CCTCCAATGT GTAAGGAACA CCACAGTGTC AGAAGGAGAG GCTTGAAGAA 1500
GATAGGTGAC TGGCCAAGGT CACATGCAGG TGAAGGAGTG GCAGAACTTG TACCCCAGAG 1560
CCCACTCTTA TAACGAGCCC TCTGTATTGG ATGGCCCCAG CAGACCCGAG AGGACAGGCC 1620
AGTGGAGAGC TCAGCATGGA GTCAGGTGGG GGAGACTCCT CTGTTCTCAG TGGAGGCCAG 1680
GCCCAGCTGT CCTGGAAGGA GCTAGAAGCC TGAATTCAGG TTGTGGAGCA GTGAGAGTCC 1740
AGCCCCACAC AGGATGCCAT GGGAGGAGGC CCTTCAAACC GGGATTCTGA AAGAACACAT 1800
CCAATAGAAG GGGCAAGGGC TGCTGAGGGC CCTGAGGAGG GGGCGTGGGC TACCCATGAG 1860
CAGGCCCTTC ACTCGTGGCC TCAGCTGCCC CTGCAGAAGG CTGGAGCCTG AGAGGAAGCC 1920
AGCCAAGTGA GCGGTGGAGG AGGAAGCTGG TCACATTCAG TTCTGGCTGA CTCACGGGAT 1980
CTGGGCTGAA GGACATATGT CTGGGAGTGC CCCAGAAAAT ATCTCACTGA TATGGGAGAT 2040
TTACTGGACT GCCTTTGGGG ATTAGGCGTA GCCTCCCTTC CCTGCACCCC AGGGAGTGAA 2100
TCCACTTCCC CACCCCTACC AGTGACCTCA GGCAGATGGC CCCAGGTAGA GAAAGCTGTG 2160
ATTTGGTCAA GGACTCCTCT TGGCAGAGGC TGGCAGACCT CTAGGCCAGC CAGAGGAGAT 2220
GGGCCTGCAG TGCACAGCCC CAAGGACTGG ACACGTGTAC ACACAGCACC CAGAGGGACA 2280
GGATGTGAGG GCCAGGCTGG GCAGATGCAG GGAAGCCTTG AAGCCACCCT TGCTCTTCTC 2340
CTCTACACCC CAAGTCCTCA GTCAACCCTG TTGGCTCCAG CTCCACAGTA CAAGCCTCTT 2400
CTGGTTCCTT TCCCACTGTC TTTTGAGCCT CCCCTTTACC AGCCTCCCTG CTTCTACCCT 2460
TGACCCAGAG TCTGTTCTCA ACACTGCAGC CAGAGTGATA GTGTTAAAGA TCACATCACT 2520
TCTGGGTTCA TTCCAGTGGG CCGTCATCCA CCCCAACTTC ACCAAGAGCA AATGCCAAGC 2580
CCCCACCTCC CAAAACATAC CTCTTAGATA CTATTTCCTA CTCCTCTCCC CATTCCTCAC 2640
TCTGCAACAG CCACTCTGGC TTTCTTGCTT TTTTTCAAAT AGCCCAGGCA CAGCCTCCCA 2700
CCCCAGGCCT TTGTACTGTC AGTTCCCTGT GCCCTGAACA CTCTTTTCTT AGACATCGGC 2760
ATGGCATACC ACCTTACTGC CTTCCAGCCT GCTCAAATAT CACTGTATTT CTCAGCATTC 2820
AAATTAGCAT TATTTCAGGA CTATTTTCAA AGGTGTGGAC AGGCTGTAAG GAAACCCTAA 2880
GGGAGAGTGC AGTGCCCAGG TTCAGTAGCA TGGGGCATTT TTGCTACTCC CAGGCCTGGC 2940
AGAAGGGCGA GGAGGAGGGA AAGACATGGC TGGTGGAAGG AAGGACAGAA TTGTGGGAGA 3000
GGGCCACCTG 3010