EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS023-24938 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr9:248240-249520 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs785836chr9248428hg19
TF binding sites/motifs
Number: 23             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:248448-248466CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr9:248440-248458TTTCCCCTCCTTCCTTCC-6.2
EWSR1-FLI1MA0149.1chr9:248482-248500CCTCTCTTTCTTCCTTCC-6.53
EWSR1-FLI1MA0149.1chr9:248427-248445CCTTCCTTCTGTCTTTCC-6.59
EWSR1-FLI1MA0149.1chr9:248498-248516CCTTGCCTCCTTCCATCC-6.62
EWSR1-FLI1MA0149.1chr9:248486-248504TCTTTCTTCCTTCCTTGC-6.81
EWSR1-FLI1MA0149.1chr9:248490-248508TCTTCCTTCCTTGCCTCC-7.02
EWSR1-FLI1MA0149.1chr9:248502-248520GCCTCCTTCCATCCTTCC-7.21
EWSR1-FLI1MA0149.1chr9:248506-248524CCTTCCATCCTTCCCTCC-7.85
EWSR1-FLI1MA0149.1chr9:248456-248474CCTTCCTTCCTCCCTCCC-8.32
EWSR1-FLI1MA0149.1chr9:248494-248512CCTTCCTTGCCTCCTTCC-8.69
EWSR1-FLI1MA0149.1chr9:248452-248470CCTTCCTTCCTTCCTCCC-9.47
EWSR1-FLI1MA0149.1chr9:248444-248462CCCTCCTTCCTTCCTTCC-9.72
ZNF263MA0528.1chr9:248440-248461TTTCCCCTCCTTCCTTCCTTC-6.14
ZNF263MA0528.1chr9:248506-248527CCTTCCATCCTTCCCTCCCTC-6.41
ZNF263MA0528.1chr9:248466-248487TCCCTCCCTCCTCTCTCCTCT-6.42
ZNF263MA0528.1chr9:248455-248476TCCTTCCTTCCTCCCTCCCTC-6.86
ZNF263MA0528.1chr9:248478-248499CTCTCCTCTCTTTCTTCCTTC-6.99
ZNF263MA0528.1chr9:248451-248472TCCTTCCTTCCTTCCTCCCTC-7.08
ZNF263MA0528.1chr9:248490-248511TCTTCCTTCCTTGCCTCCTTC-7.17
ZNF263MA0528.1chr9:248444-248465CCCTCCTTCCTTCCTTCCTTC-7.24
ZNF263MA0528.1chr9:248448-248469CCTTCCTTCCTTCCTTCCTCC-7.42
ZNF263MA0528.1chr9:248459-248480TCCTTCCTCCCTCCCTCCTCT-7.69
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_09184chr9:247605-252181CD14
SE_53654chr9:248799-249369Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9248662248835
chr9248910249110
chr9249113249403
chr9249200249450
Number: 1             
IDChromosomeStartEnd
GH09I000249chr9249101249370
Enhancer Sequence
CCTATAGTCT CCCTGGCCTG TGCCTTTTAG ACAAAACAGA TTAACATCAC CTTTAAGCCG 60
TCAATACTGA ACATTCTGTC TTTATAAGGC CTGACTCATT ACCAATTTTA TTTGGTCAAT 120
TTTACCTTCC TTGCTTTCAA AGGAACACCA TTTGCCTATG TCAAGTGTTC TCTTTCTTTT 180
ATTTTTCCCT TCCTTCTGTC TTTCCCCTCC TTCCTTCCTT CCTTCCTCCC TCCCTCCTCT 240
CTCCTCTCTT TCTTCCTTCC TTGCCTCCTT CCATCCTTCC CTCCCTCTCT CTCTTTCTTT 300
CTTTCTTTCT CTCTCTCTCT CTTTCTTTCT TTCTCTCTCT CTGTCTTTCT TTCTCTCTTT 360
CTTTCTTTCC ATCTTCTTTT CTTTCTATCT TTCTTACTTT TGATGTAGCT GTCACGACCT 420
AATGAAAATA CTGGCATGAG TGATGCCACC TTTAGATTCT CCACCTTCCT GTTCCTGTCC 480
TATTCACCAA CATGAATTGG TTTGTGGCTG TAAGTACTTG GTGGGTTATT GCTCATAGAT 540
TCAGTTGCAT TTTTGCTGAG ATAGTGCTGT TACCAAAAGC AGGGGTGCTG CTTGAAGAAG 600
TAAACCTAAC TCTGAAAAAT AGAGACTCTC CAGAAACATC ATAATCTTAA GGATGGACAT 660
TTGTGGCCTG TTATTGTTAC TTCATTCTAG GTGACAGAGT GAAGTGAGTG AGGGCAAAAA 720
TGACTGCACA CTTATGGAAA GAGGGCTGCC TCCACCACAG ACAGGTAGTG GGAGGTCCCA 780
CTCTTCCAGG TTGAACCCAA TATCCTATCT TCTCCTTCCG CTCTTGGTAC CTGTTGTTGC 840
TATTGTAAAC ACTTCCCTCA CCTGGGACTG CATATAGATG AAAGATTGCT GGGGGGTTTC 900
CCAGGATCTT GGGCCAGTGC CAACAAATGG CAAACTTTCA AGTCTAGAGA TGGTCCTATG 960
GCATGACTGG GGGACACCAC TTCCTTCACC AGAACATTCA CATCCTTCCC AAGGTGCCAC 1020
GCCCAGTTCT TTTGTCCAAC AATAAACTCT GCGAAGTGGA GTGAAGTCAC CACCCAAGCC 1080
TTAGCCTACC TCTGACCACA GCCTGTGACT CCACAAAGAT AAATGAAAAG AGGAAAGTCA 1140
GTGATGTTTT CTATACTGTC AGCAGCAATC TCACAGCCTC AATACATTTT CTTTCAAAAG 1200
TTTAATATGT AATAACTGGC ATTTCTTCTT CATTCCTAGT TGGTTAGACT GCATCACATC 1260
TGCCATGCCA AACTATTAAG 1280