EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-37648 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr2:102842690-102845160 
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
GGCTTGCAGG CTCGTAGTGA TTGAGGAAAT ATTTGCTAAG CTGCAGGAGG AGATCATCTT 60
CTAAGTCCTG CTGCAACCAT GTTACAAAAG TTTCCACGTC CATCCTCCGT CCACTGCGGG 120
AAAGTTTCTC CGAAACCAAA GTGCTCTCCA TCCATGATGT GTGCTCAGCA CAGTGGGTAC 180
TTTCTCAGAA TCTGGGTCAT GGAGAGGGAT GAGCTGCCTG CGGTTGGAGC TCTCTCTAGG 240
CCCTGTACTT GGTGCCTGAA GGGATTTAAG TCTTCAACTC TCAGATATGG AGAGAGATCA 300
AACCAAGTTT GAATGTGACT TCTCCACTTA CTCCCTATGT AAACTTAGAA AGATGTTTAA 360
CTTTCTTCTA TTTCTCAGCT ATAGAAAGGA ATAGAGGAAG GAAGGAAGGA GACAGGGAGG 420
GAGGAAAGAA AGAGAGAGAG AGGGAGGAAG GAAAGGAGAG AGGGAGGGAA AACGGAGGGA 480
AGAAGGGAGT TTCGTAGAAA AGAAACTAAA GAAAGCAGGG GAGAGAGATG GAGGAGAAGG 540
GAGGAAGGGA AGAAAGAAGG AAGGGAAGAA AAAAGAAAGA AACAAAGAAA GGGACAGTGA 600
TTAAATCCTG CTTTTTGACA GTGGGAATAA CTGAGTTGAA GTACAGGGAA GCATTCAGCG 660
GGGCCTGGGC CACAGGGCGG CCTCTATTGC TTGTCTGGAG GTCAAAACAA ATCCCCAACA 720
CCACAGCTGT GGGTTTTAGT CTGTGGGCCT ATGTCCTGCC AGTGCTGTTT GGCATAGAAA 780
TGCCTCAGTG TGATCCTGAC TCTCTGAGAG CCTGGCATTT CCCACCATGG TGCTTGTGAC 840
TATGCTACTT TTGTTTTGTT TTGTTTTGTT TTGTCTTAGA ACAGATACAA TCTATTAAGG 900
CCTTGCAAAA GTAATAAATC TGCTCTAAAG TCCCCTAATT AGATGAAAAA AGAAGCCTGG 960
TGCAGCTGAT CTGTGTGGAG ATGCACGACT TTATACCTTT TAAGTCCAGA GGCCTGAGTG 1020
ACAAGAGCAG GAAAGGGAGG GAAACTGGTT GTCTGAGAAC GTTTTATGGG CCAGCTAAAA 1080
CATAAAAGAG GTCACTGGCA TCAAGTGCTT GCTTTGCACA TAAAATACAC AGTACGGTTG 1140
TTGCCCACAT GTTTGATAAA ACGTGGCTAT TCACTAACTT GGATTTTTTC CAAATTAAAT 1200
TTCTGAATTC AGAATTAGCA ACCCTGAGCA ATGTAGAAAG CGATAAACTC CTTTTTAATG 1260
ACAAAAGTCA TCTGAACCTT AAGTGTCCAG TGCAACCTGA AGTGCTGCTA GTACTGTGGA 1320
TAGTCCGACT GGGCATGGGG AGGGGGTCTC TGGTTTTGGC TCTGGCATCT GCAGAGGCCG 1380
CCCCGTCTAA GCACACCCAT GACTGCTCTC TCCTGCTTGC GTCTTTGAGA AGAAGACAGT 1440
TCAGTCCCCC ACCACTGATT GTTTTCTGAC ACAGAGTTGA GTGGTTCAGT TGCTTTCTAC 1500
TTTTTGACTA ACAGAAGCCT GCGTCACTTT ACGTATTCTT CCTGGAAGCT CAGGCCCCAT 1560
GGTGTGTCTC TCTCACTGTC TCTCTCTCTC ACTGACTCTG TCAGTGACTC TCTCACTGAG 1620
TCATTGCGAC TCCCAGGAGC GTGACTATAG CTGTGACTTA TGGGTGTTGT GCAGTGTGTG 1680
GGGAAGCTGC TAGTGAGGTC GAGTTTAGCA GGAAGAGAAA ACAGGAATAG TGACTCACAC 1740
GGAGTAGTGG GGGCTGGGCA GATGAGAGAG TTAGGCAGCC CCGCCCTCTG CTGAGACTGG 1800
GACGCAGCCC AGATTCTGCA ACAGTGGGCA GAGGATTTGG CGATGGAGGC TAACAGGCAG 1860
CCAGGGGTCC TTTTTTTCTT TATTTTTATT TTGCTTAATT CAGAAAAGTA TGTGTGCATT 1920
TTGTGATGAA ATTCTCTACA GCTCTGTCTA CGAGAACTGC CCTGTAATAT CTCTGTGTGT 1980
TGGCTTTAAC AGTGAGCTAC TGATGAGATT CTGAGATTAG TCCCAGATCT TGTTTATGTC 2040
CTTGTTCCCC TTGAGGATAT TTTCTGAGTT AAATCAGGAA ATACCGATTA ATGGATGAAA 2100
ATGAGAAAGA GAGAAATAAT GTCCTTCGTA GGATAAGTCA TTTACCCTGA CTAGGTTAGC 2160
TAAGCTGTAT CACTCAATTA ATAATTAGGT GTGCATGACT CACCATTTTA GAAGGAGCCA 2220
TTGACAGCCC TAGCTGAAGT CAGCAAGTTC TGTATCTTCT CTAGCAAGCC ACTGGAGCTT 2280
TACAAATTCT CCTGGCAGGG GTGCATGTGT GTACGAGGAT GGAAGGGTCT GTGCACGGAT 2340
CTCCTAGAGA GATTTGAAAA TGCCTCGCCT TACTCCAGAT AGGTCTTTGG AGAATGTGCA 2400
TGTAGGATAG AATGGCTAAA ACGAAGACAA GCCAAACAGT TAGAGTGATC AAAGGGAAAC 2460
CAAGGGGACA 2470