EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS018-23257 
Organism
Homo sapiens 
Tissue/cell
CD19+ 
Coordinate
chr8:145086900-145089120 
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: 2             
ChromosomeStartEnd
chr8145087499145087624
chr8145088816145089042
Number: 1             
IDChromosomeStartEnd
GH08I144014chr8145088569145089510
Enhancer Sequence
GGCCTCGCTC CCAAGAGAGT GAGGAGGGAA GTGGGGACTG CACCAGAGAG GAGAGACTCA 60
GTGTGCTGAG GTCTCAGGAG GTCATGGAGG GAGTGCCCTT CTCCTTGCCC TCTCTGCTCT 120
AACACACTCA GCTCACCAGA CAATGTGCTT CCTGTCCTGG AGGAGGCTGC ATTCCCTCCT 180
GTCCAGGGTG GACCTCTCCA CAGGTGCTCA GAGCCCACCC ACCCCTGCGG TGACCTGCCT 240
CCATCACAGG CCCTGTACCT TGCCCTCCTT ACCTGGCCCT CTCCTCTGTC CACCATCAGG 300
TATGAAATCT TCCTCCTTCC CTGAAAGGAC ACCTCTGCTC TTTCTGGTCT CTGCTTATTT 360
AAGCCTCTAC AGCTTGGCAA CGAACCCTGA CACCACTGCT CTAGAACGGT CACAAGTGCC 420
TTCCTAGGTG CTGCATCCTT CTCCACCTCT GCATGGCATC TGAGATCGAT AGCCCTCCTC 480
CATGACCCTC TTTCTGAGTT CCCAAGCCAT CTTGTCCATC CCTCTGGCTC ATCTTAATTG 540
AGGCTGCTCC CAGGCTCTGG GTCCAGGCCC TGTCCCTCCA CCCTCAGCCA GCGTACCCAC 600
AGCGCAGCTT CAACTCTCCA CTAGAACTCA AGATCCCCTC CAGATCCTGC AGGCTCAATG 660
AGTCACTGGA ACTTAGCTCA CTCCAAACTA GACATGTTTC TGACTGATAA CTTGGGTCTT 720
TCCAGCAGCT AAAGCCCTTC AGGCTTGTGC TCACTCCCCT CCTGTCTTAA TTCCCTGCCC 780
CCTACCCACT GGGTTCCCTG CCATACAACC TGAAATGTGG CATAGGGCTG GTCTTCAGTT 840
CTCCCTTACT GATTACGAGC ACATAGACAC CTCTAGCTTT AAATGTTATA CCCCTAATGA 900
CACAGAGACA ACAGAGAGGG TAAAAAGAAT AATACACATG GGGCCAGGTG CGGTGGCTCA 960
CACCTATAAT CCCAGCACTT TGGGAAGCTG AGGCAAGCAG ATGACCTGAG GTCAGGAGTT 1020
TGAGATCAAC ATGGCCAACA TGGCGAAACG CCATCTCTAC TAAAAACACA AAAATCTTCT 1080
GGACATGGTG GTTCACGCCT ATAATCCCAG CTACTCGGGA GGCTGAGGCA GGAGAATCAC 1140
TTGAACCTGA GAGGTGGAGT TTGCAGTGAG CCAAGATCAC ACCACTGCAC TCCAGCCTGG 1200
TCAACAGAGC GAGACTCCAT CTCAAAAACT AATAATAGGC TGAGTGCAGT GGCTCAGCCC 1260
ATAATCCCAG CACTTTGGGA GGCCAAGGTG GGTGGATCAC CTGAGGTCAG GAGTTTGAGA 1320
CCAGCCTGGC CAACATAGTG AAACCCCATC TCTACTAAAA ATACAAAAAG TTAGCCAGGC 1380
GTGGTGGCAC ATGCCTGTGG TCCCAGCCAC TTGGGAGGCT GAGACAGGAG AATCCCTTGA 1440
ACTGGGAGGC AGAGGTTGCA GTGAGCCGAG GTTGCGCCAT TGCACTGCAG CCTGGGCAAA 1500
AAGAGCGAAA TTTTGAAAGA AAAAGAAGGA AAGAAAGAAA GAAAGAGAGA GAGAGAGGAA 1560
GGAAGGAAGG ATGGAAGGGA GGGAAAGGAA AAAAGAAAGA AAGAAAGAGA AAGAAAGGGA 1620
AAGGAAGGAA GGAAGGAAAA GAGAGGAGGA GGAGGAGAAG AAGAACAAGA AGAAGAAGGA 1680
GGAGGAGGAG AGGAAGAAAG AAGGAAGAAG AAGAAGAAGA AAATAAAACA AAAGAAAAGA 1740
AGAAGGAAGG AAGGAAAGAA GGAAGGAAGG AAAGAAATCT TCCTGTTTAA GAAGCTAGAC 1800
TCTGGTTTCG TACTCCCAGG CTAACCAAGC AAGCCCTCTC CTCCCAGCTT TCATTCTTAA 1860
GGGAATCCTT GGACCACTTC AGATCTTCCA ACTCCCAAAA GGTCAAGCTT TGAGGCTTAG 1920
GAAAGACTTC CTGGAGGAGG TGAGCCCAGC CAACTGGTTG TGAAGGGGAA AGGAGCGTGC 1980
CACAAGTAGA AGTGACTCAT ACAAGTGTCT GGCCCCAGGG ATTGCTGGAA TGAGAAACAG 2040
ATGTGCAATT AAAGCCCTGA CCCATGTGTG TCTCACGTGG GTGAACGTGT GTGAATGCGC 2100
TATGAGAGTA TGTGGCACAC ACTATGCACC ACACATACTC TGCAGTGTGA GTATGGAGCG 2160
TGTGGTGTGG GTGTGTGAAT GAGTGTGTAT GAATGTGTGT AGGGAAATGT GCATGATGCT 2220