EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-19709 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr15:65187570-65190710 
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: 2             
ChromosomeStartEnd
chr156518763065188212
chr156518946665189943
Number: 1             
IDChromosomeStartEnd
GH15I064891chr156518320165190998
Enhancer Sequence
CCAGAGTCTC ACTGGGGTTC TAGCCCAGCT GGGAAGTTGA GCAAAGAGGG ATAAGTGGGT 60
TACAGCTCAA GGACTGGGGG TGCCTTGGGG CTTCTAGGAG ATGAGAGCCG AAAGGCATTC 120
AGCCCTTTAA CCCCACTCCA GAGCTTCAGA CTGTTCCTTC TCAAGACACT TTACTGCCAT 180
CTGTCTGAAA AGTGTGCTAA TAAATATGCA AATTTTGGTG ACTTGAGAGG ACTGGTGTCC 240
TCTTGAGTTG TACAGGGCAC AATTTGCAGA TTTGTGAGTG ATCACCAAGC CCCGAAGATG 300
CAGCGAGGTC TCTGGCAACT CCCTTTCTCA GTCCCTTCTC TATTCCTCTC TTCTTCTTTG 360
TCCCTCTCAG ACTGGGACTG GGGGTGGGGG CAGGGGGGGG ATTTCCTACT AGGGTGGGAG 420
GAAGAAGGGT GAAGGAAGTA GGGTAGGAGG AGGGGAAGTG TGGAGGACAA CAGAGGGAAA 480
GGGTAGAACT TATTTCTGCT GTCAGAAACC GAAACCAAAA GTCCTGGCAG GAGTTAATGT 540
GAGAGGGAGG TCTGTAGCAA GAGGCTGAGG AGCAAAGCCT TCACATCTGA GGACAGCAGC 600
CCTGTCAGAG ACACCCTGGC TGCAACCTCG GTGTCACTTA GACCAGGGCT TGCCTCTCAT 660
GCTGACAAGA AGCATGCAAA GGCAGTCTGT TTTCTCTGGG GATACCAAAG GCCCCTCCAG 720
ACCTTACAGT GCCCAGCACT GGTGTTAGGA TCACTGCTGG AAAGGGGAGG GGGCACTAAC 780
TCAAGTCACC ATGTCATCTA ATAGCCCAAG AGTGGGTGAC CCTTTGTCTT GTCTGGTATT 840
AGTCTGTGTG GACCTGCATA CACCCATGAG GCTGAGGCTG GGGGCAGCCG GCATCTGTGT 900
GTCTAGCATA ATGGGGATCC TCTTTCCCCA AGTCAAGCTT AGGACGTGTG GTATAACATA 960
GATTTTTGTG ATCCACCTGG CTGTGAGAGG TCATTTAGGT GCCACAATAA TGGATTCTTT 1020
GGGGCACTTC ATACTCTATT ATAACAATAG GAGAAAATGT TTGCAACTTG GACTTGTCTT 1080
TTAAAATTCA GATTGTGTGG CCACTATTTC TTGTGAACTT TGTGATTCAA CGAGCCAATT 1140
GTGTACTGGG AACCCAGATG GTGCCCCTCC CTTGAGGCTT GCTGGGTCCT CTGTGTAGGG 1200
ATAGACTCTG TTCCGGGCGC CGTGGCTCCC AGTTCCAGAC TGGCAGCCCT TTGAGCGGCT 1260
GAAACTTTAA TTCATCTTTG TATCTCCCAT GATGATAGGA ACCTCCTGTC TCCTCAGGGG 1320
TTCTCAGAGT GTGAGTTTCT GGCTTCTCCA TTCATCCCTC TGAGGCTGAC ATATCTGTGC 1380
TGGCTTCACA GAGGCAGAGA AGAATGGGGA GCATGCAGGG GAGGTGGACT GATGGATCAG 1440
GGCACAGGGG AACCTGGCTC CACCATTTCC CAGCCCTGAG GCCTTGGACA AGTTACATTT 1500
CTGAGTCTCA GTTTCTTCAT CTGTAAATGG GGATGATTTA AATAGTTGAC TTTTACTGAG 1560
CATGTTCTCT GGGTCAGGCA CTGCGTTAAG CATATTGCAG GCAGACTTAT TCAGAAAGCA 1620
TTTATGAGGG CCTCCAATGT GTAAGGAACA CCACAGTGTC AGAAGGAGAG GCTTGAAGAA 1680
GATAGGTGAC TGGCCAAGGT CACATGCAGG TGAAGGAGTG GCAGAACTTG TACCCCAGAG 1740
CCCACTCTTA TAACGAGCCC TCTGTATTGG ATGGCCCCAG CAGACCCGAG AGGACAGGCC 1800
AGTGGAGAGC TCAGCATGGA GTCAGGTGGG GGAGACTCCT CTGTTCTCAG TGGAGGCCAG 1860
GCCCAGCTGT CCTGGAAGGA GCTAGAAGCC TGAATTCAGG TTGTGGAGCA GTGAGAGTCC 1920
AGCCCCACAC AGGATGCCAT GGGAGGAGGC CCTTCAAACC GGGATTCTGA AAGAACACAT 1980
CCAATAGAAG GGGCAAGGGC TGCTGAGGGC CCTGAGGAGG GGGCGTGGGC TACCCATGAG 2040
CAGGCCCTTC ACTCGTGGCC TCAGCTGCCC CTGCAGAAGG CTGGAGCCTG AGAGGAAGCC 2100
AGCCAAGTGA GCGGTGGAGG AGGAAGCTGG TCACATTCAG TTCTGGCTGA CTCACGGGAT 2160
CTGGGCTGAA GGACATATGT CTGGGAGTGC CCCAGAAAAT ATCTCACTGA TATGGGAGAT 2220
TTACTGGACT GCCTTTGGGG ATTAGGCGTA GCCTCCCTTC CCTGCACCCC AGGGAGTGAA 2280
TCCACTTCCC CACCCCTACC AGTGACCTCA GGCAGATGGC CCCAGGTAGA GAAAGCTGTG 2340
ATTTGGTCAA GGACTCCTCT TGGCAGAGGC TGGCAGACCT CTAGGCCAGC CAGAGGAGAT 2400
GGGCCTGCAG TGCACAGCCC CAAGGACTGG ACACGTGTAC ACACAGCACC CAGAGGGACA 2460
GGATGTGAGG GCCAGGCTGG GCAGATGCAG GGAAGCCTTG AAGCCACCCT TGCTCTTCTC 2520
CTCTACACCC CAAGTCCTCA GTCAACCCTG TTGGCTCCAG CTCCACAGTA CAAGCCTCTT 2580
CTGGTTCCTT TCCCACTGTC TTTTGAGCCT CCCCTTTACC AGCCTCCCTG CTTCTACCCT 2640
TGACCCAGAG TCTGTTCTCA ACACTGCAGC CAGAGTGATA GTGTTAAAGA TCACATCACT 2700
TCTGGGTTCA TTCCAGTGGG CCGTCATCCA CCCCAACTTC ACCAAGAGCA AATGCCAAGC 2760
CCCCACCTCC CAAAACATAC CTCTTAGATA CTATTTCCTA CTCCTCTCCC CATTCCTCAC 2820
TCTGCAACAG CCACTCTGGC TTTCTTGCTT TTTTTCAAAT AGCCCAGGCA CAGCCTCCCA 2880
CCCCAGGCCT TTGTACTGTC AGTTCCCTGT GCCCTGAACA CTCTTTTCTT AGACATCGGC 2940
ATGGCATACC ACCTTACTGC CTTCCAGCCT GCTCAAATAT CACTGTATTT CTCAGCATTC 3000
AAATTAGCAT TATTTCAGGA CTATTTTCAA AGGTGTGGAC AGGCTGTAAG GAAACCCTAA 3060
GGGAGAGTGC AGTGCCCAGG TTCAGTAGCA TGGGGCATTT TTGCTACTCC CAGGCCTGGC 3120
AGAAGGGCGA GGAGGAGGGA 3140