EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS112-00343 
Organism
Homo sapiens 
Tissue/cell
KELLY 
Coordinate
chr1:44029220-44032470 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11210871chr144029353hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr1:44031473-44031484GGGCGGGAAGG+6.62
RFX1MA0509.2chr1:44031569-44031585CGTCGCCATGGCTACC+6.63
RFX1MA0509.2chr1:44031569-44031585CGTCGCCATGGCTACC-6.63
RFX2MA0600.2chr1:44031569-44031585CGTCGCCATGGCTACC+6.51
RFX2MA0600.2chr1:44031569-44031585CGTCGCCATGGCTACC-6.75
ZfxMA0146.2chr1:44031429-44031443GGAGCCGGGGCCTG+6.13
Number of super-enhancer constituents: 22             
IDCoordinateTissue/cell
SE_00616chr1:44028518-44030367Adipose_Nuclei
SE_00616chr1:44031018-44034110Adipose_Nuclei
SE_03403chr1:44028960-44031281Brain_Angular_Gyrus
SE_03403chr1:44031827-44032190Brain_Angular_Gyrus
SE_04240chr1:44028929-44032553Brain_Anterior_Caudate
SE_05040chr1:44028789-44032962Brain_Cingulate_Gyrus
SE_05962chr1:44028621-44033904Brain_Hippocampus_Middle
SE_07193chr1:44028796-44032406Brain_Hippocampus_Middle_150
SE_08033chr1:44028848-44033378Brain_Inferior_Temporal_Lobe
SE_23829chr1:44030959-44031993Colon_Crypt_2
SE_24870chr1:44029728-44030787Colon_Crypt_3
SE_24870chr1:44031008-44032391Colon_Crypt_3
SE_26649chr1:44028759-44032143Esophagus
SE_27645chr1:44028997-44029875Fetal_Intestine
SE_27645chr1:44031458-44032280Fetal_Intestine
SE_31538chr1:44028779-44031982Gastric
SE_33537chr1:44028154-44033824H2171
SE_41575chr1:44029231-44029720LNCaP
SE_41575chr1:44029923-44031318LNCaP
SE_41575chr1:44031957-44032511LNCaP
SE_65452chr1:44028737-44032849Pancreatic_islets
SE_69138chr1:44029195-44031995H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14402925344029375
Number: 1             
IDChromosomeStartEnd
GH01I043563chr14402882644032589
Enhancer Sequence
AGAGACTGGA GGGAAACTGG GAGTGTGTGA GGTCAAGAAA TGCCAAGAGA AAAAAGTGTG 60
CGAAGGAGGA GGAGTGGTCA GCAGGGCGGG GTGCTGCCGA GAGGCCCGGC ATGTGTCCTT 120
AACAGTTAGT TCCGTGGAGC CATTGTTGGC TTTGGTGTTG GGAGACAGCA GGGCTGAGAA 180
GTGAGAGGGA GGCTATCAGT GTCTGTAGTG ACTGGAAGGG CCCGAACCTA GGGAGTGAAT 240
GGATGACAAG AGTCTCCCTG GAGTAGGACT GAGGTTGGGG AGCCACTGAA GGAGAGTCCA 300
GTGTGGGCCC GAGTCTGGAA CTCCAGTGTG GGTCGGGTGT ATGCGCAGGG CATGGCCCCT 360
GGGTTCTTGT GGTGGGGAGG CCTCAACTGG GTTGAGTAGG GCGATGTGGG GTGCCAGGGA 420
AACCCGAGGA AGGAGGGGAT GACTGGGAGG GGGACGCCGT GCCTGCCAAC AGGCCCCAAA 480
CAGCTCAGAT TGAAAAACAA AACAGGCTTT TAAGATGCCA AGTTTGATGA AATCTGAGTG 540
CTGGAAGAGG TGGGAGTTTG CTCTTGGAAA AACAGCTGAA AATCGAGACT CAAAGCTGCG 600
AAGGGAGATG GGCCCAAGGC TCCCCAGGCC CCCCTTACTG CCTGGAAGCC TGGGGGTGGG 660
GCTGGGCTCT CTGGGAGAGT GTGGGAGCGT GCAGATCTGG CAGCCTTCGA CTTTTGGAAG 720
GCGTCTGGCT CTGGCCCTGC TGAGGATGGA GCTGCTGGAG GTGGCCTTGG CTTCTGTGGA 780
GCGGCTGAAG GGCAGGGGGA GCCAGCAGCC CTGCCACCTA CGAGGTTCCT TCATGTGTCT 840
CGTCCCTGCA TGTGTCTCCA GGCGCACGTG TTTTGGCATA GGTGTGTCTG GCTGTGCATG 900
TCTCCACATG TGTGTTTGCG TGTCTCTGTG TGCACCGCCT CTGGATCTGC TTGCATGCGC 960
CTGTTTCCAC AGGTGCTAGT CACTGCAGGT GCCCCTCCAC ATGCACATGT AGGTTTCTAT 1020
TTTTACACCT GTCTGTTTCT CCATGTATAT TTCTGTGGGT TCCTGGCTGT GCATGTTTCT 1080
ATGGTGTCTG TGTGTTGAGA GGCAGGGTGA GGCCAGGCCC AACACTCAAG CTTAGGGGAG 1140
GCGGTCAGGC TCACAGACGG TGCCACCCCA GGGGGCCTGT GTCTGTGTGT GCGGGTGCGT 1200
GCCTGCGTTT GCACGGAGAC GCCACGAAGC TGGGTAAACA TGGGTGAAAA GGTCATACTG 1260
ACAGACGGTG CTGCCTGCCC CAGGACCCTG CAAGGCGTCT CCATCTGTCA GCTTCCCTGG 1320
TGCAGCCCCC TCCCTCTGGC CCAGAGACTC ACCCTCAGGC GTCCAAGGCT GAGCTGGACA 1380
AAGAGACCTG TGTGTACTTT GTAGGGGGCC TCAGCAGCCT CCACCCCCAT CTTAGGCTCC 1440
TCTGTCAGGA CCCCAACACA TGCCCCAGCT CCCACCAGAC TCGCCTTGGT ACTGTCATCC 1500
CACCACCTTC CCCCACAACA GCCTTTACAA AGGCAGTTTT CCCCTCCTCC CTGGAAAGCT 1560
TTCTGCCTCC CATGCTCATG TGTTTCCTGT TCTTGAATCT CCCTCCTCCA GGAAGCCACC 1620
AAGATAGCAA GTGAGCTGTG GAGTCAAACC GATCAGCTCC AACACTGCTG TGGGAGGTTA 1680
GCCAAGCGCT CATCCACTTC TGAACCTTGG ATTCCCACCA TCGACCCCCG ACCCTCCCCT 1740
CGCTAGGGCT TGTCATCGTC TTCTGCCCAT GGGGCAACCA AACCTCTCCA CGGAAGGGGA 1800
CAGGTCTCCT TGCTGCAGTG GGTAAAGGCC AGCGCAGTTA GGTGCAGGAG GCATTCACAC 1860
ACACGTGCAC ACTCCCCACC TTGCACACAT ATCTGCGTGA GCCGGGGAGA CCCTAGGGAA 1920
TGTGTGTGCA TGTTGTCTAT GCATGCGGGT AGAATCCGCA AACGGTGTGG AGACTCGGGC 1980
TCTTGGGTAC CTCTGAAGGC CCCTGAAGTC CCCATGGGCT TCTCCTTCCG TCCAGGGCAC 2040
CCTCTTATCA GGCCATGGCC CTGAGACGCG TAGTGCAGAC GCCCCCGGCG CTGAGGCTGA 2100
GGAGGCAGAT GGCCCCTCCC CGCACTGTGC AGGGCACCCG GTTGGGGGTG GAGGGGAGGG 2160
CCGCGTCGGT GAAGCGGGAA AGCCTAGTGG GAGGATTCCC TGGAGCTGAG GAGCCGGGGC 2220
CTGGGAAGGG GCGCAGAGGC TCCACCCAGG CGGGGGCGGG AAGGGCGGTG CCAGGGCGGA 2280
CAGCGGACGC GCGCGCCTGC ACGGACTCGG GCACACGCAG CCCTTCCGCG GCAGCGCCCG 2340
CCGCTCCACC GTCGCCATGG CTACCGGCTG GCCTGGAGCG GGGAGGGGCC CTTCCTCCCC 2400
TTCGGCGCCA ACAGGAGGCG ATTTGAGGGG ACTCAGCGTG ACTGGTGCAT CCCGGGGTTG 2460
GAAAATGGGT GGGTGCTTGC GACTGTCCAC GTGTGGGGGA CCCTGGGGTT CGCTTTGCGG 2520
TAGATGCAAA CGCCGCGGCG CGTGTGCGGG GCTCTGCAGT GGAGCCTGAG CCGTGCCGGC 2580
CGAGGCGTGG TGTGGGGGAG GCTGCCGGCC CTCTCGCGCG CGGGGTGTTC ACGCCTAGAG 2640
CGCTGGGGCT GGGGGCCTAC CACCCGGTCT CCTCCCAGCC CCACCTCCGA TTTAGCTGTG 2700
TGACCTTGGG CAGGTGTCCA GATGTCTAGA TCTCTCTCAG CCCCTGGTTG CCCATGTACC 2760
TCATAAGGGT TTGGTAAAGA TTTAAGTCAT TTTGTAAAGC ATTTTAACAT AGTACCTGGA 2820
ACCTAGTAAA TGCTTCATAA ATCTTACTGT CCCTCATACC TGGGTCTCAG TTTTCCCAGT 2880
TGTTGATGGG TTTGGAGTGA TCATGTGACA TCATCTGAGG AGTTGCCCAG GTCCTCAGCC 2940
TGAGTGTTGA GGCTGCGGTA GACCCAGCTT CCGCGGGTGC CCGTGGGGGA AGGTGGTAAG 3000
TGTGCCAGTC TGGCTGATAG ATCAGTTTAC ACCAGGATGC CCAGTGCTCA GCCAGGCCAG 3060
GCGCATGGTG GGCGTCAGGA AAGGGCTGCT GTACTTGGCT GAGTTGAATG TTCAGAGGCG 3120
CCTGGATGGG AGAGAAGGAA GAGGCAGCAG CAAGTCGCTC CTGAGGGGCT GGAGCCCTCC 3180
TGTAAGACCC ACTTCCCTTC CCGGGTGGCA GAGTGGCAGA CTTCCGAGTG CTGCCTAGAA 3240
GCCTAGTTGG 3250