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

TagContent
EnhancerAtlas ID
HS187-13722 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr2:102842550-102845600 
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: 4             
ChromosomeStartEnd
chr2102843334102845009
chr2102842650102845550
chr2102844840102845062
chr2102844003102844653
Number: 1             
IDChromosomeStartEnd
GH02I102226chr2102842670102846324
Enhancer Sequence
TACATATACA ACGATTTCAA ATATACTTTG TCATATTTTA CTACGTTGTT GGCAAATTTA 60
GGGAAAGGAA TCTCCTTGGA ACTGCCTGTG CTTTAGAGAA ATGATTTGTC CCTAATCACC 120
AGCATCATTT GGTCAGATAA GGCTTGCAGG CTCGTAGTGA TTGAGGAAAT ATTTGCTAAG 180
CTGCAGGAGG AGATCATCTT CTAAGTCCTG CTGCAACCAT GTTACAAAAG TTTCCACGTC 240
CATCCTCCGT CCACTGCGGG AAAGTTTCTC CGAAACCAAA GTGCTCTCCA TCCATGATGT 300
GTGCTCAGCA CAGTGGGTAC TTTCTCAGAA TCTGGGTCAT GGAGAGGGAT GAGCTGCCTG 360
CGGTTGGAGC TCTCTCTAGG CCCTGTACTT GGTGCCTGAA GGGATTTAAG TCTTCAACTC 420
TCAGATATGG AGAGAGATCA AACCAAGTTT GAATGTGACT TCTCCACTTA CTCCCTATGT 480
AAACTTAGAA AGATGTTTAA CTTTCTTCTA TTTCTCAGCT ATAGAAAGGA ATAGAGGAAG 540
GAAGGAAGGA GACAGGGAGG GAGGAAAGAA AGAGAGAGAG AGGGAGGAAG GAAAGGAGAG 600
AGGGAGGGAA AACGGAGGGA AGAAGGGAGT TTCGTAGAAA AGAAACTAAA GAAAGCAGGG 660
GAGAGAGATG GAGGAGAAGG GAGGAAGGGA AGAAAGAAGG AAGGGAAGAA AAAAGAAAGA 720
AACAAAGAAA GGGACAGTGA TTAAATCCTG CTTTTTGACA GTGGGAATAA CTGAGTTGAA 780
GTACAGGGAA GCATTCAGCG GGGCCTGGGC CACAGGGCGG CCTCTATTGC TTGTCTGGAG 840
GTCAAAACAA ATCCCCAACA CCACAGCTGT GGGTTTTAGT CTGTGGGCCT ATGTCCTGCC 900
AGTGCTGTTT GGCATAGAAA TGCCTCAGTG TGATCCTGAC TCTCTGAGAG CCTGGCATTT 960
CCCACCATGG TGCTTGTGAC TATGCTACTT TTGTTTTGTT TTGTTTTGTT TTGTCTTAGA 1020
ACAGATACAA TCTATTAAGG CCTTGCAAAA GTAATAAATC TGCTCTAAAG TCCCCTAATT 1080
AGATGAAAAA AGAAGCCTGG TGCAGCTGAT CTGTGTGGAG ATGCACGACT TTATACCTTT 1140
TAAGTCCAGA GGCCTGAGTG ACAAGAGCAG GAAAGGGAGG GAAACTGGTT GTCTGAGAAC 1200
GTTTTATGGG CCAGCTAAAA CATAAAAGAG GTCACTGGCA TCAAGTGCTT GCTTTGCACA 1260
TAAAATACAC AGTACGGTTG TTGCCCACAT GTTTGATAAA ACGTGGCTAT TCACTAACTT 1320
GGATTTTTTC CAAATTAAAT TTCTGAATTC AGAATTAGCA ACCCTGAGCA ATGTAGAAAG 1380
CGATAAACTC CTTTTTAATG ACAAAAGTCA TCTGAACCTT AAGTGTCCAG TGCAACCTGA 1440
AGTGCTGCTA GTACTGTGGA TAGTCCGACT GGGCATGGGG AGGGGGTCTC TGGTTTTGGC 1500
TCTGGCATCT GCAGAGGCCG CCCCGTCTAA GCACACCCAT GACTGCTCTC TCCTGCTTGC 1560
GTCTTTGAGA AGAAGACAGT TCAGTCCCCC ACCACTGATT GTTTTCTGAC ACAGAGTTGA 1620
GTGGTTCAGT TGCTTTCTAC TTTTTGACTA ACAGAAGCCT GCGTCACTTT ACGTATTCTT 1680
CCTGGAAGCT CAGGCCCCAT GGTGTGTCTC TCTCACTGTC TCTCTCTCTC ACTGACTCTG 1740
TCAGTGACTC TCTCACTGAG TCATTGCGAC TCCCAGGAGC GTGACTATAG CTGTGACTTA 1800
TGGGTGTTGT GCAGTGTGTG GGGAAGCTGC TAGTGAGGTC GAGTTTAGCA GGAAGAGAAA 1860
ACAGGAATAG TGACTCACAC GGAGTAGTGG GGGCTGGGCA GATGAGAGAG TTAGGCAGCC 1920
CCGCCCTCTG CTGAGACTGG GACGCAGCCC AGATTCTGCA ACAGTGGGCA GAGGATTTGG 1980
CGATGGAGGC TAACAGGCAG CCAGGGGTCC TTTTTTTCTT TATTTTTATT TTGCTTAATT 2040
CAGAAAAGTA TGTGTGCATT TTGTGATGAA ATTCTCTACA GCTCTGTCTA CGAGAACTGC 2100
CCTGTAATAT CTCTGTGTGT TGGCTTTAAC AGTGAGCTAC TGATGAGATT CTGAGATTAG 2160
TCCCAGATCT TGTTTATGTC CTTGTTCCCC TTGAGGATAT TTTCTGAGTT AAATCAGGAA 2220
ATACCGATTA ATGGATGAAA ATGAGAAAGA GAGAAATAAT GTCCTTCGTA GGATAAGTCA 2280
TTTACCCTGA CTAGGTTAGC TAAGCTGTAT CACTCAATTA ATAATTAGGT GTGCATGACT 2340
CACCATTTTA GAAGGAGCCA TTGACAGCCC TAGCTGAAGT CAGCAAGTTC TGTATCTTCT 2400
CTAGCAAGCC ACTGGAGCTT TACAAATTCT CCTGGCAGGG GTGCATGTGT GTACGAGGAT 2460
GGAAGGGTCT GTGCACGGAT CTCCTAGAGA GATTTGAAAA TGCCTCGCCT TACTCCAGAT 2520
AGGTCTTTGG AGAATGTGCA TGTAGGATAG AATGGCTAAA ACGAAGACAA GCCAAACAGT 2580
TAGAGTGATC AAAGGGAAAC CAAGGGGACA ATGGGAAAAC AAGTCGGGGT AGAGTTAATG 2640
ACACCTTTAA CAATTATTAA AGGTGAATTT GCTTTTCAAG CTAAAGCAAA GGCAATGACA 2700
AGATCCACTG TGTGCCATTC ACAACAACCT TTCAGATTTT CATGAGAGAA CATGGCTTTT 2760
TCTGAGACTA ATTTCCAAAG GCAGATTTTT TTTCCCCCAC AGGGAGTCCT CATTTCAAAA 2820
GGGCATGGTG TAGGGAAGCT TGACTGCAAC AACTTTCCCA TGGTAAATGT CATAGCGTGT 2880
TTTGTGTGGC TTTTCTTCTA GTGTTTTCTA TGCATATTGG GGGTAAACCC ACCAAACCTC 2940
CTGCAGTTCA GTAAAAGCAT TTGCGTGGAG GCCAGATTGA ATCTGAATTT TCCACTGTTC 3000
TGGTTTCATC AGGCCTAAAA TTTAGCAATA TCATATTGAG AGAAAGTAGG 3050