EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS102-02618 
Organism
Homo sapiens 
Tissue/cell
HuCCT1 
Coordinate
chr1:230886210-230887780 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs61828378chr1230887224hg19
TF binding sites/motifs
Number: 29             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:230887255-230887273GGAAGGAAGGAGAGAAAG+6.94
EWSR1-FLI1MA0149.1chr1:230887219-230887237GAAGGGAAGGGAGGAAGG+7.28
EWSR1-FLI1MA0149.1chr1:230887251-230887269AGAAGGAAGGAAGGAGAG+7.37
EWSR1-FLI1MA0149.1chr1:230887223-230887241GGAAGGGAGGAAGGGAGG+8.06
EWSR1-FLI1MA0149.1chr1:230887227-230887245GGGAGGAAGGGAGGAAGG+8.37
EWSR1-FLI1MA0149.1chr1:230887235-230887253GGGAGGAAGGAAGGAAAG+8.84
EWSR1-FLI1MA0149.1chr1:230887239-230887257GGAAGGAAGGAAAGAAGG+9.09
EWSR1-FLI1MA0149.1chr1:230887243-230887261GGAAGGAAAGAAGGAAGG+9.17
EWSR1-FLI1MA0149.1chr1:230887247-230887265GGAAAGAAGGAAGGAAGG+9.47
EWSR1-FLI1MA0149.1chr1:230887231-230887249GGAAGGGAGGAAGGAAGG+9.6
FOSL2MA0478.1chr1:230886569-230886580GGGTGACTCAG+6.02
FOXP1MA0481.2chr1:230887511-230887523AGGTAAACAGAA+6.14
IRF1MA0050.2chr1:230887263-230887284GGAGAGAAAGAGAAAGAAAGA-6.48
IRF1MA0050.2chr1:230887345-230887366AGAAAGAAAGAGAAAGAAAGA-6.76
JUNBMA0490.1chr1:230886569-230886580GGGTGACTCAG+6.02
ZNF263MA0528.1chr1:230887233-230887254AAGGGAGGAAGGAAGGAAAGA+6.02
ZNF263MA0528.1chr1:230887237-230887258GAGGAAGGAAGGAAAGAAGGA+6.06
ZNF263MA0528.1chr1:230887215-230887236GAAGGAAGGGAAGGGAGGAAG+6.14
ZNF263MA0528.1chr1:230887187-230887208GAAGGAGAGGAAGAGAGAGAG+6.17
ZNF263MA0528.1chr1:230887212-230887233AGGGAAGGAAGGGAAGGGAGG+6.21
ZNF263MA0528.1chr1:230887192-230887213AGAGGAAGAGAGAGAGGGAAA+6.42
ZNF263MA0528.1chr1:230887225-230887246AAGGGAGGAAGGGAGGAAGGA+6.66
ZNF263MA0528.1chr1:230887236-230887257GGAGGAAGGAAGGAAAGAAGG+6.89
ZNF263MA0528.1chr1:230887240-230887261GAAGGAAGGAAAGAAGGAAGG+6.93
ZNF263MA0528.1chr1:230887256-230887277GAAGGAAGGAGAGAAAGAGAA+6.93
ZNF263MA0528.1chr1:230887295-230887316AAAGGAAGAAGAGAAAGAAAG+6
ZNF263MA0528.1chr1:230887602-230887623GGGGGAGGGGAGGGGGAGGGG+7.49
ZNF263MA0528.1chr1:230887228-230887249GGAGGAAGGGAGGAAGGAAGG+7.61
ZNF263MA0528.1chr1:230887607-230887628AGGGGAGGGGGAGGGGGAGGG+8.24
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_32194chr1:230882390-230887232Gastric
SE_32194chr1:230887396-230890088Gastric
SE_33557chr1:230879014-230891230H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1230886279230886687
chr1230886815230887110
Number: 1             
IDChromosomeStartEnd
GH01I230750chr1230885992230891172
Enhancer Sequence
CAGATTTCTG TAAAATCAGG AACAAAAGGG CTGAGGATGA GCATGGAGAC TCTTCTTGCA 60
GCATAGAGTC GCAGGGAGCC GGGGGGTAGC GGGCCATAGG GAAATCACAA GCATTGCCAG 120
GTTCCCTGCA GACCTCTGTG GCTTGGGCAT CATTTGCAGT GGGACTCAGC ATTACACGGT 180
GCACATCTCA GCAGCCCGTG GGACCGTGGG GCTGGACGGC CCTCCTCCTC AGCACCACCT 240
TCTTGTCAAA CACAGCTGTA CTTGGGGAGG GTGGGCAGAG CACAAAGCCA AGGGGACATT 300
GGAGGGCAGT GGACAGCCAG GCTTGCCCTC AAGGGAGCCC AGGGCAAGGA GTGCACTGAG 360
GGTGACTCAG GGAACTGGCT GGGAGGGGCT GGGAGGCAGA GAGGGTGATA GGCTCAACCT 420
GGAGAGAAGG TGAGATCACC CCCAGGTCTC ATGCAAGGGA CTGTGGACCT GAGTGGAAGT 480
GGGTGCACAG AAAGAGGAGG AGGGAGTATC GGGTGAGGTC TCCCAGCCTG ATGGGGAACA 540
GCCACCATGC AGTCCATCCC TCCTTGTCTG CCTGTACCCA TTTATTTTTG GCCAGGCAAT 600
TCCCCCCCAC CAATTCTCAG TGTAAATCCA GGACACCTCC CCGAAAGTGC CCACACCCCT 660
CTAGCCCATG TGAACAACCC CTGTGGCAGA CCTGTGCACA GCGTGGCATG TGACCACAGC 720
CTCTCCTGCA CGGTGAGCTT GCCGTTCCCT GTGCTGCTCC CCTGACCCCC AGGAGGGGTT 780
GTCAGTTGTT CTGGGACAGC CCCAAAGGCC CCATGGCCTC CACAGTGCTG GGCACATGAC 840
AGGGATCGGC ACATAGCTAT GAACAGCAGC GTCTGGCATC TCCAGACCTT GCTGGAAATG 900
TGGCTTTTCT TCACTGGAAG GCCATGTGAA AGACAGAATG AATGAAAAAG AAAGAGAGAA 960
AGAAAGAGAA AAAGAGAGAA GGAGAGGAAG AGAGAGAGGG AAAGGGAAGG AAGGGAAGGG 1020
AGGAAGGGAG GAAGGAAGGA AAGAAGGAAG GAAGGAGAGA AAGAGAAAGA AAGATAGAAA 1080
AAAAGAAAGG AAGAAGAGAA AGAAAGAAAG AAGAAAGAAA CAAAGAAAGA AAGAAAGAAA 1140
GAAAGAGAAA GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA 1200
AAGAAAGAAA GAAAGAAAGA AGGGTGGCTT TTCCCTTTGT GAATTATTCA CTGTGCTTAG 1260
TAGAGGAAAG TGTGTCTTCG GCTGAGCCCC GATGATGTAC AAGGTAAACA GAACAGTCCC 1320
TGAAAGCAAA CATTCCAGGG TGCTTGGCCC TTAGTGCTCC AGGAAAACCA CCTGGTGGTA 1380
GGGCTGTGGG GTGGGGGAGG GGAGGGGGAG GGGGAGGGGT CTGCGTGCCT CCCTCGGGGC 1440
TTCAGGCAGC AGTCTAGGTT CACTTCAGGT TTGTCAAGAC CCCTGCAATT GAGACACCTC 1500
TGATCGTCCT ATCACAGGAC TGTAGCTTCA GGTAACCCCT TCCTCATGGC CTCCCAAGCA 1560
ACATTTCACA 1570