EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-04967 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr11:2913120-2914400 
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:2913183-2913201CCTTCCTCCCTCCCATTC-6.1
EWSR1-FLI1MA0149.1chr11:2913829-2913847CCCTCCTCCCCTCCCTCC-6.34
EWSR1-FLI1MA0149.1chr11:2913159-2913177AACTCCTTCCTTCTTTCC-6.37
EWSR1-FLI1MA0149.1chr11:2913179-2913197CATTCCTTCCTCCCTCCC-7.39
EWSR1-FLI1MA0149.1chr11:2913844-2913862TCCTCCTTCCTTCCCTCC-7.41
EWSR1-FLI1MA0149.1chr11:2913163-2913181CCTTCCTTCTTTCCTTCA-7.69
EWSR1-FLI1MA0149.1chr11:2913167-2913185CCTTCTTTCCTTCATTCC-7.69
EWSR1-FLI1MA0149.1chr11:2913175-2913193CCTTCATTCCTTCCTCCC-7.85
EWSR1-FLI1MA0149.1chr11:2913171-2913189CTTTCCTTCATTCCTTCC-8.84
ZNF263MA0528.1chr11:2913829-2913850CCCTCCTCCCCTCCCTCCTCC-10.97
ZNF263MA0528.1chr11:2913189-2913210TCCCTCCCATTCTCCACCTCC-6.02
ZNF263MA0528.1chr11:2913171-2913192CTTTCCTTCATTCCTTCCTCC-6.1
ZNF263MA0528.1chr11:2913811-2913832CCTCTCTGCTCCCCCTGCCCC-6.1
ZNF263MA0528.1chr11:2913174-2913195TCCTTCATTCCTTCCTCCCTC-6.49
ZNF263MA0528.1chr11:2913186-2913207TCCTCCCTCCCATTCTCCACC-6.51
ZNF263MA0528.1chr11:2913183-2913204CCTTCCTCCCTCCCATTCTCC-6.66
ZNF263MA0528.1chr11:2913192-2913213CTCCCATTCTCCACCTCCTCC-6.79
ZNF263MA0528.1chr11:2913836-2913857CCCCTCCCTCCTCCTTCCTTC-6.7
ZNF263MA0528.1chr11:2913876-2913897TCCTCTTCCTCTTCCTGCCCT-6.94
ZNF263MA0528.1chr11:2913847-2913868TCCTTCCTTCCCTCCTCATCC-7.02
ZNF263MA0528.1chr11:2913817-2913838TGCTCCCCCTGCCCCTCCTCC-7.14
ZNF263MA0528.1chr11:2913820-2913841TCCCCCTGCCCCTCCTCCCCT-7.62
ZNF263MA0528.1chr11:2913844-2913865TCCTCCTTCCTTCCCTCCTCA-7.84
ZNF263MA0528.1chr11:2913832-2913853TCCTCCCCTCCCTCCTCCTTC-9.71
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_52971chr11:2913184-2914673Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1129134872914258
Number: 1             
IDChromosomeStartEnd
GH11I002889chr1129103402914767
Enhancer Sequence
ACCTCCAGGG TCAGAGAAGG AGGGGAGCCC CCAACACTTA ACTCCTTCCT TCTTTCCTTC 60
ATTCCTTCCT CCCTCCCATT CTCCACCTCC TCCTGGCTGA GCTTTGAAGC CAGGGCAGTT 120
GGCCAGACCG AGCGCAGAGG CCAGGAGGTG ACGGCAGGCT TGCCCTGGCG GCCTCCCAGG 180
TTAACACACT CCCAGGTGGC TGCACCCCAC AGGCGAGGGC TGCTCAGAGT AGATGCTCAA 240
CCAAGAGGTT GCCCGTGCCC CCTTCCCCAG CCGCAGGGGC AGCCAGAAGC CAAGCAGCCT 300
CCCGCCCACT GGAGCCTGGA GCCTGAGGGC TGAAGCTGGG CGCCTGCTGC CCCCTGGCGT 360
CCCGAAACGG CACAGCCACC AGGACCCCCA CCCACCTCAT TCATGCCTCA CACCTGGGGG 420
TGACTTGGGC CAGGGCCTTG CTCTCTGGCC CCGAGTCCCC TCAAGTGTAA GATGGGGGCT 480
CTGCCCAGTG TGGCTGTCCG GGCTGCAGCG GGCAGGAGCG CATTTTTCAC AAACCCCAAC 540
ACCCCTCGGA TCTGGGGGTG GGGCGGTGTC ACTCGCACCT CAGTGGGAAA CAGCACGTGG 600
GCCTCGCCCG TCTCCAGGGG GTGGGGGAGG GGAGACAAAG AGCCCGCTCT GCGGAGAGGT 660
GGGTACCCGC CCTGCCGCCC CTCCCCCATT TCCTCTCTGC TCCCCCTGCC CCTCCTCCCC 720
TCCCTCCTCC TTCCTTCCCT CCTCATCCCC AGCTCCTCCT CTTCCTCTTC CTGCCCTATC 780
CCCCCGCAGG CCCGGCCGGC AGCCCGGCGC CCTCTGCCTT CGTTCCCGCC ATTGGCGCTG 840
CTGCCCGGAG CCCCTAGGTG ACAGCCAGCC CCGAGGCTGC AGCCTCTGTG TCGGGCCTGC 900
ACCTGCCCAC CGCGTGGTCA CTGCCTGGGC ACGTATGGAC ACTCACACCC TTCAGTCCTG 960
AGCACAACTG TGCCCTGGCT GCTTCGGAAC AACAAGGAAT CATAGTCCTG CTTCTGGCTG 1020
GGAGCTGGGG GCCAGCAATC AGGGCAGCTG GGGAAGTGGT TAGGGAGGTG GCGGCACACA 1080
GGCCGAGCTC AGAGAGTGAG CAGAGAATGG GCCCAGGGGA GGGCGCTGGA GAGGGCTGCA 1140
GGGCTTGGGG CTGCAGCTCA GGAGCTGGCT TCACCTTGGA GGCTATCAGA CCTGCTCCTC 1200
AGCATTGGCC CAGCAAGGGG AACAGTATGG GGAACAGGGG ACAGGCACTG CCTGGCCAGC 1260
AGCAAACAAG TAGGCTGTGG 1280