EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS026-33682 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr8:145088030-145089450 
TF binding sites/motifs
Number: 33             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr8:145088448-145088466GAGAGAGAGGAAGGAAGG+6.25
EWSR1-FLI1MA0149.1chr8:145088660-145088678GGAAGGAAGGAAAGAAAT+7.43
EWSR1-FLI1MA0149.1chr8:145088464-145088482GGAAGGATGGAAGGGAGG+7.83
EWSR1-FLI1MA0149.1chr8:145088452-145088470GAGAGGAAGGAAGGAAGG+8.32
EWSR1-FLI1MA0149.1chr8:145088640-145088658AGAAGGAAGGAAGGAAAG+8.46
EWSR1-FLI1MA0149.1chr8:145088656-145088674AGAAGGAAGGAAGGAAAG+8.46
EWSR1-FLI1MA0149.1chr8:145088522-145088540GGAAGGAAGGAAGGAAAA+9.07
EWSR1-FLI1MA0149.1chr8:145088460-145088478GGAAGGAAGGATGGAAGG+9.09
EWSR1-FLI1MA0149.1chr8:145088644-145088662GGAAGGAAGGAAAGAAGG+9.09
EWSR1-FLI1MA0149.1chr8:145088648-145088666GGAAGGAAAGAAGGAAGG+9.17
EWSR1-FLI1MA0149.1chr8:145088652-145088670GGAAAGAAGGAAGGAAGG+9.47
EWSR1-FLI1MA0149.1chr8:145088456-145088474GGAAGGAAGGAAGGATGG+9.55
EWSR1-FLI1MA0149.1chr8:145088518-145088536GAAAGGAAGGAAGGAAGG+9.6
IRF1MA0050.2chr8:145088483-145088504AAAGGAAAAAAGAAAGAAAGA-6.19
IRF1MA0050.2chr8:145088497-145088518AGAAAGAAAGAGAAAGAAAGG-6.59
JUN(var.2)MA0489.1chr8:145088886-145088900TAGAAGTGACTCAT+6
ZNF263MA0528.1chr8:145088457-145088478GAAGGAAGGAAGGATGGAAGG+6.12
ZNF263MA0528.1chr8:145088547-145088568GGAGGAGGAGAAGAAGAACAA+6.14
ZNF263MA0528.1chr8:145088638-145088659GAAGAAGGAAGGAAGGAAAGA+6.22
ZNF263MA0528.1chr8:145088596-145088617AAAGAAGGAAGAAGAAGAAGA+6.27
ZNF263MA0528.1chr8:145088461-145088482GAAGGAAGGATGGAAGGGAGG+6.42
ZNF263MA0528.1chr8:145088641-145088662GAAGGAAGGAAGGAAAGAAGG+6.45
ZNF263MA0528.1chr8:145088465-145088486GAAGGATGGAAGGGAGGGAAA+6.8
ZNF263MA0528.1chr8:145088645-145088666GAAGGAAGGAAAGAAGGAAGG+6.93
ZNF263MA0528.1chr8:145088583-145088604GGAGGAGAGGAAGAAAGAAGG+7.05
ZNF263MA0528.1chr8:145088599-145088620GAAGGAAGAAGAAGAAGAAGA+7.37
ZNF263MA0528.1chr8:145088568-145088589GAAGAAGAAGGAGGAGGAGGA+7.39
ZNF263MA0528.1chr8:145088571-145088592GAAGAAGGAGGAGGAGGAGAG+7.97
ZNF263MA0528.1chr8:145088541-145088562AGAGGAGGAGGAGGAGAAGAA+8.43
ZNF263MA0528.1chr8:145088580-145088601GGAGGAGGAGAGGAAGAAAGA+8.43
ZNF263MA0528.1chr8:145088574-145088595GAAGGAGGAGGAGGAGAGGAA+8.68
ZNF263MA0528.1chr8:145088577-145088598GGAGGAGGAGGAGAGGAAGAA+8.6
ZNF263MA0528.1chr8:145088544-145088565GGAGGAGGAGGAGAAGAAGAA+8.98
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8145088816145089042
Number: 1             
IDChromosomeStartEnd
GH08I144014chr8145088569145089510
Enhancer Sequence
GGAGAATCAC TTGAACCTGA GAGGTGGAGT TTGCAGTGAG CCAAGATCAC ACCACTGCAC 60
TCCAGCCTGG TCAACAGAGC GAGACTCCAT CTCAAAAACT AATAATAGGC TGAGTGCAGT 120
GGCTCAGCCC ATAATCCCAG CACTTTGGGA GGCCAAGGTG GGTGGATCAC CTGAGGTCAG 180
GAGTTTGAGA CCAGCCTGGC CAACATAGTG AAACCCCATC TCTACTAAAA ATACAAAAAG 240
TTAGCCAGGC GTGGTGGCAC ATGCCTGTGG TCCCAGCCAC TTGGGAGGCT GAGACAGGAG 300
AATCCCTTGA ACTGGGAGGC AGAGGTTGCA GTGAGCCGAG GTTGCGCCAT TGCACTGCAG 360
CCTGGGCAAA AAGAGCGAAA TTTTGAAAGA AAAAGAAGGA AAGAAAGAAA GAAAGAGAGA 420
GAGAGAGGAA GGAAGGAAGG ATGGAAGGGA GGGAAAGGAA AAAAGAAAGA AAGAAAGAGA 480
AAGAAAGGGA AAGGAAGGAA GGAAGGAAAA GAGAGGAGGA GGAGGAGAAG AAGAACAAGA 540
AGAAGAAGGA GGAGGAGGAG AGGAAGAAAG AAGGAAGAAG AAGAAGAAGA AAATAAAACA 600
AAAGAAAAGA AGAAGGAAGG AAGGAAAGAA GGAAGGAAGG AAAGAAATCT TCCTGTTTAA 660
GAAGCTAGAC TCTGGTTTCG TACTCCCAGG CTAACCAAGC AAGCCCTCTC CTCCCAGCTT 720
TCATTCTTAA GGGAATCCTT GGACCACTTC AGATCTTCCA ACTCCCAAAA GGTCAAGCTT 780
TGAGGCTTAG GAAAGACTTC CTGGAGGAGG TGAGCCCAGC CAACTGGTTG TGAAGGGGAA 840
AGGAGCGTGC CACAAGTAGA AGTGACTCAT ACAAGTGTCT GGCCCCAGGG ATTGCTGGAA 900
TGAGAAACAG ATGTGCAATT AAAGCCCTGA CCCATGTGTG TCTCACGTGG GTGAACGTGT 960
GTGAATGCGC TATGAGAGTA TGTGGCACAC ACTATGCACC ACACATACTC TGCAGTGTGA 1020
GTATGGAGCG TGTGGTGTGG GTGTGTGAAT GAGTGTGTAT GAATGTGTGT AGGGAAATGT 1080
GCATGATGCT GACTCTGGGC ATACTGCCTA GGAGTTAGCG TTTCTCACAA GGAGCGGTGC 1140
TGTCAAAAGA AAATTAAATG TAATTTTTAA ATATTTAAAA TTTTTTTTTT TTTGAGAGAC 1200
AGAGTCTTGC TCTGTCACCC AGGCTGGAGT GCAGTGGCAC AATATCAGCT CACTGCAACC 1260
TCTGCTTCCT GGGTTAAAGT GATTCTCCTG CCTCAGCCTC CTGAGTAGCT GGGATTACAG 1320
GTGCATGCCA GTACTCCTGG CTAATTTTTT TTTTTTTGGT GTATTTTTAG TAGAGATGGA 1380
GTTTCACCAA GCTGGCCACA CTGGTCTCAA ACTTCTGACC 1420