EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-26916 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr2:102842680-102845540 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1997502chr2102844249hg19
TF binding sites/motifs
Number: 22             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:102843224-102843242AGAAGGGAGGAAGGGAAG+6.05
EWSR1-FLI1MA0149.1chr2:102843104-102843122GGGAGGGAGGAAAGAAAG+6.23
EWSR1-FLI1MA0149.1chr2:102843228-102843246GGGAGGAAGGGAAGAAAG+6.25
EWSR1-FLI1MA0149.1chr2:102843127-102843145GAGAGGGAGGAAGGAAAG+6.42
EWSR1-FLI1MA0149.1chr2:102843232-102843250GGAAGGGAAGAAAGAAGG+6.62
EWSR1-FLI1MA0149.1chr2:102843236-102843254GGGAAGAAAGAAGGAAGG+6.72
EWSR1-FLI1MA0149.1chr2:102843081-102843099TAGAGGAAGGAAGGAAGG+6.84
EWSR1-FLI1MA0149.1chr2:102843077-102843095GGAATAGAGGAAGGAAGG+7.01
EWSR1-FLI1MA0149.1chr2:102843085-102843103GGAAGGAAGGAAGGAGAC+7.67
ZNF263MA0528.1chr2:102843245-102843266GAAGGAAGGGAAGAAAAAAGA+6.06
ZNF263MA0528.1chr2:102843141-102843162AAAGGAGAGAGGGAGGGAAAA+6.09
ZNF263MA0528.1chr2:102843090-102843111GAAGGAAGGAGACAGGGAGGG+6.17
ZNF263MA0528.1chr2:102843216-102843237GATGGAGGAGAAGGGAGGAAG+6.25
ZNF263MA0528.1chr2:102843106-102843127GAGGGAGGAAAGAAAGAGAGA+6.3
ZNF263MA0528.1chr2:102843226-102843247AAGGGAGGAAGGGAAGAAAGA+6.64
ZNF263MA0528.1chr2:102843713-102843734AGAGCAGGAAAGGGAGGGAAA+6.65
ZNF263MA0528.1chr2:102843094-102843115GAAGGAGACAGGGAGGGAGGA+6.7
ZNF263MA0528.1chr2:102843132-102843153GGAGGAAGGAAAGGAGAGAGG+6.94
ZNF263MA0528.1chr2:102843229-102843250GGAGGAAGGGAAGAAAGAAGG+7.06
ZNF263MA0528.1chr2:102843219-102843240GGAGGAGAAGGGAGGAAGGGA+7.12
ZNF263MA0528.1chr2:102843222-102843243GGAGAAGGGAGGAAGGGAAGA+7.12
ZNF263MA0528.1chr2:102843129-102843150GAGGGAGGAAGGAAAGGAGAG+7.51
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr2102843334102845009
chr2102844840102845062
chr2102844003102844653
Number: 1             
IDChromosomeStartEnd
GH02I102226chr2102842670102846324
Enhancer Sequence
GGTCAGATAA GGCTTGCAGG CTCGTAGTGA TTGAGGAAAT ATTTGCTAAG CTGCAGGAGG 60
AGATCATCTT CTAAGTCCTG CTGCAACCAT GTTACAAAAG TTTCCACGTC CATCCTCCGT 120
CCACTGCGGG AAAGTTTCTC CGAAACCAAA GTGCTCTCCA TCCATGATGT GTGCTCAGCA 180
CAGTGGGTAC TTTCTCAGAA TCTGGGTCAT GGAGAGGGAT GAGCTGCCTG CGGTTGGAGC 240
TCTCTCTAGG CCCTGTACTT GGTGCCTGAA GGGATTTAAG TCTTCAACTC TCAGATATGG 300
AGAGAGATCA AACCAAGTTT GAATGTGACT TCTCCACTTA CTCCCTATGT AAACTTAGAA 360
AGATGTTTAA CTTTCTTCTA TTTCTCAGCT ATAGAAAGGA ATAGAGGAAG GAAGGAAGGA 420
GACAGGGAGG GAGGAAAGAA AGAGAGAGAG AGGGAGGAAG GAAAGGAGAG AGGGAGGGAA 480
AACGGAGGGA AGAAGGGAGT TTCGTAGAAA AGAAACTAAA GAAAGCAGGG GAGAGAGATG 540
GAGGAGAAGG GAGGAAGGGA AGAAAGAAGG AAGGGAAGAA AAAAGAAAGA AACAAAGAAA 600
GGGACAGTGA TTAAATCCTG CTTTTTGACA GTGGGAATAA CTGAGTTGAA GTACAGGGAA 660
GCATTCAGCG GGGCCTGGGC CACAGGGCGG CCTCTATTGC TTGTCTGGAG GTCAAAACAA 720
ATCCCCAACA CCACAGCTGT GGGTTTTAGT CTGTGGGCCT ATGTCCTGCC AGTGCTGTTT 780
GGCATAGAAA TGCCTCAGTG TGATCCTGAC TCTCTGAGAG CCTGGCATTT CCCACCATGG 840
TGCTTGTGAC TATGCTACTT TTGTTTTGTT TTGTTTTGTT TTGTCTTAGA ACAGATACAA 900
TCTATTAAGG CCTTGCAAAA GTAATAAATC TGCTCTAAAG TCCCCTAATT AGATGAAAAA 960
AGAAGCCTGG TGCAGCTGAT CTGTGTGGAG ATGCACGACT TTATACCTTT TAAGTCCAGA 1020
GGCCTGAGTG ACAAGAGCAG GAAAGGGAGG GAAACTGGTT GTCTGAGAAC GTTTTATGGG 1080
CCAGCTAAAA CATAAAAGAG GTCACTGGCA TCAAGTGCTT GCTTTGCACA TAAAATACAC 1140
AGTACGGTTG TTGCCCACAT GTTTGATAAA ACGTGGCTAT TCACTAACTT GGATTTTTTC 1200
CAAATTAAAT TTCTGAATTC AGAATTAGCA ACCCTGAGCA ATGTAGAAAG CGATAAACTC 1260
CTTTTTAATG ACAAAAGTCA TCTGAACCTT AAGTGTCCAG TGCAACCTGA AGTGCTGCTA 1320
GTACTGTGGA TAGTCCGACT GGGCATGGGG AGGGGGTCTC TGGTTTTGGC TCTGGCATCT 1380
GCAGAGGCCG CCCCGTCTAA GCACACCCAT GACTGCTCTC TCCTGCTTGC GTCTTTGAGA 1440
AGAAGACAGT TCAGTCCCCC ACCACTGATT GTTTTCTGAC ACAGAGTTGA GTGGTTCAGT 1500
TGCTTTCTAC TTTTTGACTA ACAGAAGCCT GCGTCACTTT ACGTATTCTT CCTGGAAGCT 1560
CAGGCCCCAT GGTGTGTCTC TCTCACTGTC TCTCTCTCTC ACTGACTCTG TCAGTGACTC 1620
TCTCACTGAG TCATTGCGAC TCCCAGGAGC GTGACTATAG CTGTGACTTA TGGGTGTTGT 1680
GCAGTGTGTG GGGAAGCTGC TAGTGAGGTC GAGTTTAGCA GGAAGAGAAA ACAGGAATAG 1740
TGACTCACAC GGAGTAGTGG GGGCTGGGCA GATGAGAGAG TTAGGCAGCC CCGCCCTCTG 1800
CTGAGACTGG GACGCAGCCC AGATTCTGCA ACAGTGGGCA GAGGATTTGG CGATGGAGGC 1860
TAACAGGCAG CCAGGGGTCC TTTTTTTCTT TATTTTTATT TTGCTTAATT CAGAAAAGTA 1920
TGTGTGCATT TTGTGATGAA ATTCTCTACA GCTCTGTCTA CGAGAACTGC CCTGTAATAT 1980
CTCTGTGTGT TGGCTTTAAC AGTGAGCTAC TGATGAGATT CTGAGATTAG TCCCAGATCT 2040
TGTTTATGTC CTTGTTCCCC TTGAGGATAT TTTCTGAGTT AAATCAGGAA ATACCGATTA 2100
ATGGATGAAA ATGAGAAAGA GAGAAATAAT GTCCTTCGTA GGATAAGTCA TTTACCCTGA 2160
CTAGGTTAGC TAAGCTGTAT CACTCAATTA ATAATTAGGT GTGCATGACT CACCATTTTA 2220
GAAGGAGCCA TTGACAGCCC TAGCTGAAGT CAGCAAGTTC TGTATCTTCT CTAGCAAGCC 2280
ACTGGAGCTT TACAAATTCT CCTGGCAGGG GTGCATGTGT GTACGAGGAT GGAAGGGTCT 2340
GTGCACGGAT CTCCTAGAGA GATTTGAAAA TGCCTCGCCT TACTCCAGAT AGGTCTTTGG 2400
AGAATGTGCA TGTAGGATAG AATGGCTAAA ACGAAGACAA GCCAAACAGT TAGAGTGATC 2460
AAAGGGAAAC CAAGGGGACA ATGGGAAAAC AAGTCGGGGT AGAGTTAATG ACACCTTTAA 2520
CAATTATTAA AGGTGAATTT GCTTTTCAAG CTAAAGCAAA GGCAATGACA AGATCCACTG 2580
TGTGCCATTC ACAACAACCT TTCAGATTTT CATGAGAGAA CATGGCTTTT TCTGAGACTA 2640
ATTTCCAAAG GCAGATTTTT TTTCCCCCAC AGGGAGTCCT CATTTCAAAA GGGCATGGTG 2700
TAGGGAAGCT TGACTGCAAC AACTTTCCCA TGGTAAATGT CATAGCGTGT TTTGTGTGGC 2760
TTTTCTTCTA GTGTTTTCTA TGCATATTGG GGGTAAACCC ACCAAACCTC CTGCAGTTCA 2820
GTAAAAGCAT TTGCGTGGAG GCCAGATTGA ATCTGAATTT 2860