EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS062-02566 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr11:2912120-2914520 
TF binding sites/motifs
Number: 25             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:2913183-2913201CCTTCCTCCCTCCCATTC-6.1
EWSR1-FLI1MA0149.1chr11:2913829-2913847CCCTCCTCCCCTCCCTCC-6.34
EWSR1-FLI1MA0149.1chr11:2913159-2913177AACTCCTTCCTTCTTTCC-6.37
EWSR1-FLI1MA0149.1chr11:2913179-2913197CATTCCTTCCTCCCTCCC-7.39
EWSR1-FLI1MA0149.1chr11:2913844-2913862TCCTCCTTCCTTCCCTCC-7.41
EWSR1-FLI1MA0149.1chr11:2913163-2913181CCTTCCTTCTTTCCTTCA-7.69
EWSR1-FLI1MA0149.1chr11:2913167-2913185CCTTCTTTCCTTCATTCC-7.69
EWSR1-FLI1MA0149.1chr11:2913175-2913193CCTTCATTCCTTCCTCCC-7.85
EWSR1-FLI1MA0149.1chr11:2913171-2913189CTTTCCTTCATTCCTTCC-8.84
ZNF263MA0528.1chr11:2913829-2913850CCCTCCTCCCCTCCCTCCTCC-10.97
ZNF263MA0528.1chr11:2913189-2913210TCCCTCCCATTCTCCACCTCC-6.02
ZNF263MA0528.1chr11:2913171-2913192CTTTCCTTCATTCCTTCCTCC-6.1
ZNF263MA0528.1chr11:2913811-2913832CCTCTCTGCTCCCCCTGCCCC-6.1
ZNF263MA0528.1chr11:2912832-2912853CACCCCACCACTCCCTCCTCC-6.45
ZNF263MA0528.1chr11:2913174-2913195TCCTTCATTCCTTCCTCCCTC-6.49
ZNF263MA0528.1chr11:2913186-2913207TCCTCCCTCCCATTCTCCACC-6.51
ZNF263MA0528.1chr11:2913183-2913204CCTTCCTCCCTCCCATTCTCC-6.66
ZNF263MA0528.1chr11:2913192-2913213CTCCCATTCTCCACCTCCTCC-6.79
ZNF263MA0528.1chr11:2913836-2913857CCCCTCCCTCCTCCTTCCTTC-6.7
ZNF263MA0528.1chr11:2913876-2913897TCCTCTTCCTCTTCCTGCCCT-6.94
ZNF263MA0528.1chr11:2913847-2913868TCCTTCCTTCCCTCCTCATCC-7.02
ZNF263MA0528.1chr11:2913817-2913838TGCTCCCCCTGCCCCTCCTCC-7.14
ZNF263MA0528.1chr11:2913820-2913841TCCCCCTGCCCCTCCTCCCCT-7.62
ZNF263MA0528.1chr11:2913844-2913865TCCTCCTTCCTTCCCTCCTCA-7.84
ZNF263MA0528.1chr11:2913832-2913853TCCTCCCCTCCCTCCTCCTTC-9.71
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_52971chr11:2913184-2914673Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1129127702913342
chr1129134872914258
Number: 1             
IDChromosomeStartEnd
GH11I002889chr1129103402914767
Enhancer Sequence
CAGGGACTGC CTTGTGCTGG GGGTTCCGGC CAGGGGTCCT CACTCCCCAG GAACCGATGG 60
GCGGAGCTGG GCAGGCCCTG AGGAGAGGCC CAGTGGGAAT AGGGAACAGT CACCCCTGCT 120
CCAGAACGGG ACCAGGGGCT GCTTCCCTTG GGGTCTGGAA GAGAGGGACC CCCTGGTCCC 180
AGCCTGCCTG AGACTGCTGG TTTCGGCACT GAATGTTCCA GGAAACCGAG GGCCACTGGT 240
CATCGTGGGC TTCACACGGC GCCTTTCTGG GCTAGGAAGG GGGCTCCCGG GCTAGGAAGC 300
AGGTACCGAG GAGGGTCTCA AGGACATGTG GGGACCTATG TCAGACACCC CTGCAGCCAG 360
CTCTGAGCCC ACCAGGCCTT TCCTCCTCTC CCTGCCAATC CACAGGACAC AGACACAGGG 420
GTCCCAGGCC CAGTGGCTCA CTTTATCAGG GAAACAGCAG GAAAAACAAA TCTGGTGTGA 480
GCAGATCTCC CTTCCCACCA AGCCCCCTGA CTTCCTGCTG GAGCTCGGGG AGACCCCTGT 540
GACCAGCATC TCCTGCCTAC GGGGGGCGCC AGGGCCTCAA AGCCTCTCCA AGCCACTCCC 600
TCCCACCCTG CTTTCCACAC CCAAGCCACA GCGTTCAGAG AAGCTCAGGG CCTATTTGAA 660
ATGCCAGAGA GTGGGGATGC CTCCAGAGAG GTGGCATGAG GGCCCCCAGA TGCACCCCAC 720
CACTCCCTCC TCCACTGCAG GAGGAGGGGC CTGCAGTTAC TGAGGAAGCC TCACCCCTAC 780
TGGGCCCTCG GGGGTGAAGG GGCTTCCCAG GCCTTGAGGG AGACTGTATT TCAGATGTCA 840
GTTAAAAGCG CCTGCTACAT GGCGTGACCT CTCTGAATCC TATTACTTTC CTGTGCAGGA 900
AACTGAGGCC CAGAGAGGTG GAGTGACCGG CCTAGGGTCC CCCAGCAAGT CAGAGACAGT 960
GAAGCCACCT CCTGCCCTGG GCTGGGGTCC CGCCCCACTG ACCTCCAGGG TCAGAGAAGG 1020
AGGGGAGCCC CCAACACTTA ACTCCTTCCT TCTTTCCTTC ATTCCTTCCT CCCTCCCATT 1080
CTCCACCTCC TCCTGGCTGA GCTTTGAAGC CAGGGCAGTT GGCCAGACCG AGCGCAGAGG 1140
CCAGGAGGTG ACGGCAGGCT TGCCCTGGCG GCCTCCCAGG TTAACACACT CCCAGGTGGC 1200
TGCACCCCAC AGGCGAGGGC TGCTCAGAGT AGATGCTCAA CCAAGAGGTT GCCCGTGCCC 1260
CCTTCCCCAG CCGCAGGGGC AGCCAGAAGC CAAGCAGCCT CCCGCCCACT GGAGCCTGGA 1320
GCCTGAGGGC TGAAGCTGGG CGCCTGCTGC CCCCTGGCGT CCCGAAACGG CACAGCCACC 1380
AGGACCCCCA CCCACCTCAT TCATGCCTCA CACCTGGGGG TGACTTGGGC CAGGGCCTTG 1440
CTCTCTGGCC CCGAGTCCCC TCAAGTGTAA GATGGGGGCT CTGCCCAGTG TGGCTGTCCG 1500
GGCTGCAGCG GGCAGGAGCG CATTTTTCAC AAACCCCAAC ACCCCTCGGA TCTGGGGGTG 1560
GGGCGGTGTC ACTCGCACCT CAGTGGGAAA CAGCACGTGG GCCTCGCCCG TCTCCAGGGG 1620
GTGGGGGAGG GGAGACAAAG AGCCCGCTCT GCGGAGAGGT GGGTACCCGC CCTGCCGCCC 1680
CTCCCCCATT TCCTCTCTGC TCCCCCTGCC CCTCCTCCCC TCCCTCCTCC TTCCTTCCCT 1740
CCTCATCCCC AGCTCCTCCT CTTCCTCTTC CTGCCCTATC CCCCCGCAGG CCCGGCCGGC 1800
AGCCCGGCGC CCTCTGCCTT CGTTCCCGCC ATTGGCGCTG CTGCCCGGAG CCCCTAGGTG 1860
ACAGCCAGCC CCGAGGCTGC AGCCTCTGTG TCGGGCCTGC ACCTGCCCAC CGCGTGGTCA 1920
CTGCCTGGGC ACGTATGGAC ACTCACACCC TTCAGTCCTG AGCACAACTG TGCCCTGGCT 1980
GCTTCGGAAC AACAAGGAAT CATAGTCCTG CTTCTGGCTG GGAGCTGGGG GCCAGCAATC 2040
AGGGCAGCTG GGGAAGTGGT TAGGGAGGTG GCGGCACACA GGCCGAGCTC AGAGAGTGAG 2100
CAGAGAATGG GCCCAGGGGA GGGCGCTGGA GAGGGCTGCA GGGCTTGGGG CTGCAGCTCA 2160
GGAGCTGGCT TCACCTTGGA GGCTATCAGA CCTGCTCCTC AGCATTGGCC CAGCAAGGGG 2220
AACAGTATGG GGAACAGGGG ACAGGCACTG CCTGGCCAGC AGCAAACAAG TAGGCTGTGG 2280
AGTTGGGCAG AGCATCTGCC TCTTACTAGC TGTGTGTCCT TGGGCAAGTT GCTTAACCTC 2340
TCTGTGCCTC TTCTTTCTCA TCTGTAAAGC TTCTGATGAG GCTTAAAGGG CAAGTCAGTA 2400