EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS074-10035 
Organism
Homo sapiens 
Tissue/cell
GM19239 
Coordinate
chr22:25481400-25483080 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs5760842chr2225482991hg19
TF binding sites/motifs
Number: 29             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE41MA0636.1chr22:25481941-25481951GTCACGTGAC+6.02
BHLHE41MA0636.1chr22:25481941-25481951GTCACGTGAC-6.02
EWSR1-FLI1MA0149.1chr22:25481752-25481770GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr22:25481756-25481774GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr22:25481775-25481793GGAAGGGAGGAAGGCTGT+6.36
EWSR1-FLI1MA0149.1chr22:25481767-25481785GGGAGGGAGGAAGGGAGG+6.88
EWSR1-FLI1MA0149.1chr22:25481743-25481761GGGAGGAAGGGAGGGAGG+6.92
EWSR1-FLI1MA0149.1chr22:25481747-25481765GGAAGGGAGGGAGGGAGG+7.08
EWSR1-FLI1MA0149.1chr22:25481763-25481781GGGAGGGAGGGAGGAAGG+7.28
EWSR1-FLI1MA0149.1chr22:25481731-25481749TGAAGGAAGGAAGGGAGG+7.79
EWSR1-FLI1MA0149.1chr22:25481739-25481757GGAAGGGAGGAAGGGAGG+8.06
EWSR1-FLI1MA0149.1chr22:25481771-25481789GGGAGGAAGGGAGGAAGG+8.37
EWSR1-FLI1MA0149.1chr22:25481735-25481753GGAAGGAAGGGAGGAAGG+9.83
HNF1AMA0046.2chr22:25482102-25482117CATTAATCATTTACA+6.14
HNF1BMA0153.2chr22:25482103-25482116ATTAATCATTTAC-6.71
RELMA0101.1chr22:25482668-25482678GGAAATCCCC-6.02
ZNF263MA0528.1chr22:25481769-25481790GAGGGAGGAAGGGAGGAAGGC+6.39
ZNF263MA0528.1chr22:25481729-25481750GGTGAAGGAAGGAAGGGAGGA+6.49
ZNF263MA0528.1chr22:25481745-25481766GAGGAAGGGAGGGAGGGAGGG+6.54
ZNF263MA0528.1chr22:25481736-25481757GAAGGAAGGGAGGAAGGGAGG+6.93
ZNF263MA0528.1chr22:25481749-25481770AAGGGAGGGAGGGAGGGAGGG+7.05
ZNF263MA0528.1chr22:25481761-25481782GAGGGAGGGAGGGAGGAAGGG+7.19
ZNF263MA0528.1chr22:25481741-25481762AAGGGAGGAAGGGAGGGAGGG+7.27
ZNF263MA0528.1chr22:25481732-25481753GAAGGAAGGAAGGGAGGAAGG+7.39
ZNF263MA0528.1chr22:25481765-25481786GAGGGAGGGAGGAAGGGAGGA+7.6
ZNF263MA0528.1chr22:25481753-25481774GAGGGAGGGAGGGAGGGAGGG+7.97
ZNF263MA0528.1chr22:25481744-25481765GGAGGAAGGGAGGGAGGGAGG+7.9
ZNF263MA0528.1chr22:25481757-25481778GAGGGAGGGAGGGAGGGAGGA+8.08
ZNF740MA0753.2chr22:25481473-25481486CCTCCCCCCCCAT+6
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_01653chr22:25480325-25483006Aorta
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr222548190825483023
Number: 1             
IDChromosomeStartEnd
GH22I025085chr222548168725483037
Enhancer Sequence
CTCACTCACC AAACCCTCCC TCTGGTGTAT ATTTCCAGCA GTTTCTCTCT CCCAGTGTGC 60
TGAGGGGCCC CCACCTCCCC CCCCATAACC CCCTGTCCGT CCTGCGGCTC TGTAGGAGGG 120
ACGTGTTGCC TGCTGCTGGG AGCTTTTGAG GAACCATTGG GTGGGTCCTC ATGGCCCTGA 180
CAGGAACCAA ATGATGCTCA CCCTGTGTGT GTGAGCTGGT GTGTCTATGA CTTCCTTCAG 240
ATCCAGGCCT GGGATTCATT CCTCTGCCTC CGCACAGCCT GATAGACAGT AAGTGTCCAA 300
TATATGTTGA GTGAAGCAAA CTGATAAGTG GTGAAGGAAG GAAGGGAGGA AGGGAGGGAG 360
GGAGGGAGGG AGGGAGGAAG GGAGGAAGGC TGTTCAAGAG CAGAGATTCT CTCGTATGCA 420
CATCTGTGTC CCTGACACAT AGTAGGCACT CAATAAATAC TCACTGCACT GGAGGAATGA 480
AAGAATGAAT GGATGAGTGA GACTCTTTGC AAGCAGAAAC AGCCCCTATC TTTGTATCCC 540
TGTCACGTGA CACAGTGCCT GACATCCAGG AGTTTCCATC AATGAATGTT ATGCTGAATG 600
AATGAATGAA CCACTGAAGT GAACTCTATC AGTAGTGGCT GTGTCTTGTT TCATATCTAT 660
ATGCACAGTG CTTAGCAGAG GGCTGAGTAC ACAGCAAGTG CTCATTAATC ATTTACAGAA 720
CTGAATGAAA GAGTGAAAGA AAACAATGAA TGCGAAAATG AAACTTTTCA TCCTCAGAGA 780
GCATGTCTTG TTCATCTCTG TCTCTCCACT TCCTAGCTTA AGGTCTTGCA CACAGCAGGT 840
GCTCATTAAA TGTTAATCTG AATGAGCGAA TGAGTGGGTG AGTGAAAAAG TGGTTCTTGT 900
GGGTAGGGAC ATGTCTTGCT CATTAGTTTC CCCACTTCCT AGAACAGGGC TTGGCACACA 960
ATAGGTGCTG AATAAATAAA TATGTGTTGA GCTGAACGCA GGAGTGAGTG AGTGCATAAA 1020
TGAACTTCTT GAGGAGAGGA ATGTATCTCG TTCATCTTTT CCCTCAGATC CTAATGCAGG 1080
GCCAGGCATA GAGCAGGTGC TTAGCAAATG CTTCCTGCAC TGCCCTGACC TTTGTAGGAG 1140
CATCCATCTG TGAATGAATT GAGAAGGGAA GCCCAGCTGG GTGGACCTCG CCCATCTCCA 1200
TCTGCCCCGT CCCATCCACC CAACCCCACT GCAGACTTTT CCTGTTGTTC GGTCTGCACA 1260
GGTGGACAGG AAATCCCCCA AAGGCCGGCC AGAGAGCTGT TTCCATATTT TCTCCACACC 1320
AGGCTGGCTC TGAGTGTGAC CAAGGCGCCA GTCCGAATCC CAGCGCCGTC TGGCTGTGGA 1380
ACAGTAACCC CCAGGGACCC CTCTTCCTGA CCATGTTAGC AGTTCTAAAT TTAGAGCCGG 1440
CTGAGCAGCT TGCACCAGGC AAGTAAAGCC GGGGAATGTT CTACTCACAG CCAGCCTAAA 1500
GTTACCATGT TCAGCACTGG CCAGGCCTGT TAACCCCCAA ACAGCTGAGC AGTAGGCATG 1560
GAGAGAAGAG TTAAGGCTTT GGGGTGCAAC GGAACAGGGT TCAAATCTAC CTCTTTGACT 1620
TCAAATTTAG AATCCATGAC AACAAAAATC ACTTATGTGA GCCTCAGTTT TTCTCATCTG 1680