EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-08999 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr11:2912860-2914380 
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
GAGGAGGGGC CTGCAGTTAC TGAGGAAGCC TCACCCCTAC TGGGCCCTCG GGGGTGAAGG 60
GGCTTCCCAG GCCTTGAGGG AGACTGTATT TCAGATGTCA GTTAAAAGCG CCTGCTACAT 120
GGCGTGACCT CTCTGAATCC TATTACTTTC CTGTGCAGGA AACTGAGGCC CAGAGAGGTG 180
GAGTGACCGG CCTAGGGTCC CCCAGCAAGT CAGAGACAGT GAAGCCACCT CCTGCCCTGG 240
GCTGGGGTCC CGCCCCACTG ACCTCCAGGG TCAGAGAAGG AGGGGAGCCC CCAACACTTA 300
ACTCCTTCCT TCTTTCCTTC ATTCCTTCCT CCCTCCCATT CTCCACCTCC TCCTGGCTGA 360
GCTTTGAAGC CAGGGCAGTT GGCCAGACCG AGCGCAGAGG CCAGGAGGTG ACGGCAGGCT 420
TGCCCTGGCG GCCTCCCAGG TTAACACACT CCCAGGTGGC TGCACCCCAC AGGCGAGGGC 480
TGCTCAGAGT AGATGCTCAA CCAAGAGGTT GCCCGTGCCC CCTTCCCCAG CCGCAGGGGC 540
AGCCAGAAGC CAAGCAGCCT CCCGCCCACT GGAGCCTGGA GCCTGAGGGC TGAAGCTGGG 600
CGCCTGCTGC CCCCTGGCGT CCCGAAACGG CACAGCCACC AGGACCCCCA CCCACCTCAT 660
TCATGCCTCA CACCTGGGGG TGACTTGGGC CAGGGCCTTG CTCTCTGGCC CCGAGTCCCC 720
TCAAGTGTAA GATGGGGGCT CTGCCCAGTG TGGCTGTCCG GGCTGCAGCG GGCAGGAGCG 780
CATTTTTCAC AAACCCCAAC ACCCCTCGGA TCTGGGGGTG GGGCGGTGTC ACTCGCACCT 840
CAGTGGGAAA CAGCACGTGG GCCTCGCCCG TCTCCAGGGG GTGGGGGAGG GGAGACAAAG 900
AGCCCGCTCT GCGGAGAGGT GGGTACCCGC CCTGCCGCCC CTCCCCCATT TCCTCTCTGC 960
TCCCCCTGCC CCTCCTCCCC TCCCTCCTCC TTCCTTCCCT CCTCATCCCC AGCTCCTCCT 1020
CTTCCTCTTC CTGCCCTATC CCCCCGCAGG CCCGGCCGGC AGCCCGGCGC CCTCTGCCTT 1080
CGTTCCCGCC ATTGGCGCTG CTGCCCGGAG CCCCTAGGTG ACAGCCAGCC CCGAGGCTGC 1140
AGCCTCTGTG TCGGGCCTGC ACCTGCCCAC CGCGTGGTCA CTGCCTGGGC ACGTATGGAC 1200
ACTCACACCC TTCAGTCCTG AGCACAACTG TGCCCTGGCT GCTTCGGAAC AACAAGGAAT 1260
CATAGTCCTG CTTCTGGCTG GGAGCTGGGG GCCAGCAATC AGGGCAGCTG GGGAAGTGGT 1320
TAGGGAGGTG GCGGCACACA GGCCGAGCTC AGAGAGTGAG CAGAGAATGG GCCCAGGGGA 1380
GGGCGCTGGA GAGGGCTGCA GGGCTTGGGG CTGCAGCTCA GGAGCTGGCT TCACCTTGGA 1440
GGCTATCAGA CCTGCTCCTC AGCATTGGCC CAGCAAGGGG AACAGTATGG GGAACAGGGG 1500
ACAGGCACTG CCTGGCCAGC 1520