EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

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EnhancerAtlas ID
HS165-08639 
Organism
Homo sapiens 
Tissue/cell
Ramos 
Coordinate
chr2:233988840-233990310 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:233989937-233989955GGAGAGAAGGAAGGACAG+6.13
EWSR1-FLI1MA0149.1chr2:233989933-233989951GGGAGGAGAGAAGGAAGG+6.94
ZNF263MA0528.1chr2:233989931-233989952GGGGGAGGAGAGAAGGAAGGA+7.11
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_09311chr2:233988600-233990755CD14
SE_10919chr2:233986191-233991593CD20
SE_20168chr2:233988759-233990188CD56
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2233989200233990127
Number: 1             
IDChromosomeStartEnd
GH02I233124chr2233988782233990284
Enhancer Sequence
AGGCTTATTT CCTAAAAGAA AACCATGAGA TACCTAACCG GGCCCCTCAG TTGGCCAGGG 60
CTCTTCCTGA ATTCCAGCAG GTGGAGACTA CCAGGTCCCC CAGGCTCTCC CCGAAGAGAG 120
GAGAGATTTG TCCACAGACG CTGAGACCCT TGCCTGGCTC CTGCCTGTTC TGGGGGCTTG 180
CTGCAGGCAT CCTTTTTCTC CCTCACCTGT GGGCTGGCTT GTGGGCCACC AGGGCCCCCT 240
GCTCCCTCCC ACCCTCATGG AAACACACTT TTCATGGTTG TGCAGCTGTT CGTTTCCAAA 300
AGGACCGCAG CTCCATGGAG GCTGAAAGGG TCCCAGGCAG GCCCTGTCCC TTTTGGCCTC 360
CCTGGTCTGA GTGAGCACTG CCCTCTGGAA TCAGGAAGGT CAGGCTGTGG AAGAACTAGG 420
GCTGACCTGT CCCATTGTGA GCCCAAGGTC ACTCACCAGC ACCGCGCCCT GGCTGCACCT 480
GAACAGCTGC CCCCAGGCGC CCAGGGCCAT GCTGAGAAGC TGTTCTGCAG AAACGCCCTC 540
CACACTAAAC ACCCTCACTC CCCTCGGGCT GCCCATCCCA GCTAGTTGGG CCCCTCTGGG 600
CATGGCTGTC TGGAGGAAGA TCCCGACAAG TTTCTGTGAG GGCTGAAAAA AGAACCTCAG 660
TCTCATGACT GCTGGCTTCA CTTCCGCAAA CGAGGTCGCC CAGTTGTCGG CTCGAACCAG 720
AGCAATGCGA CATGAGGCCC GCGCAGTCCA AGAGGTCTGT TTGGGCCCAG GGCCTCTTGA 780
GGCACCGCCA GACCGTGGAG CTCGAAGCAG ACTCCTAGTT GTCTTCAGAA CCCCAGACAG 840
AGGAAGTGAA GGGCCTGTTC TCTAAAGAGG AGGTCCCCCG GGGCCCACTG TGGTTGGGCC 900
AGAGGCAGCC GCTCTGTGTG GGAAGAGGCT CAGACAGAGC TCTGGACCCT CCATTCGTGT 960
ACGTACAGAA TGAACCTTCT CCTAAAGGCG ATGGGTGGGC TCCCACCTCC CAGGCCAAGT 1020
TCAAGTCATT TGTTGAATGT CTCTGAGTGA AGGGAACCCC CTCGCTTTCT TTTATGTGTT 1080
TCTGAGAGTC TGGGGGAGGA GAGAAGGAAG GACAGAGGCT GGAGAGAGGG GACCAGGGAG 1140
AGAGGGAGAG GGGCAGTGTG GCTAGGCCTG CCTGTCTCCT TACCCCTGGT CCCCTTCCAT 1200
GGTTTTGGCC TATTCTGGGA ACTGGGCCTC TGCCTAGCCC AGGGCTCAGC CATCATGAGA 1260
CAGGTGTCTC AGCCCCTGAA AGTCTGAGAG CCAGACTCAT CCTGCTCACC TGCCTGCTGC 1320
TGTGGGCTTA GTCCATCCAA GGTCAGCAGC CCTGCAGGCC TTCCAGACCC TCCATGGAGC 1380
AAGGCCTTTT GGCCCTGGCA GGTGTTTGCT GATGGCCACA GTGGGGCAGA CACTGCACTA 1440
GCCAGGGCCC TGTGGCAGGA GGCTCTCCCT 1470