EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-11471 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr19:45266270-45267980 
TF binding sites/motifs
Number: 23             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:45267410-45267428GGAAGGAAGGAAGGAAGC+10.05
EWSR1-FLI1MA0149.1chr19:45267386-45267404GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:45267390-45267408GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:45267394-45267412GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:45267398-45267416GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:45267402-45267420GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:45267406-45267424GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:45267365-45267383GGAAGGGAGGAAAGAGGG+6.98
EWSR1-FLI1MA0149.1chr19:45267418-45267436GGAAGGAAGCAAGCGAGG+7.04
EWSR1-FLI1MA0149.1chr19:45267382-45267400GAGAGGAAGGAAGGAAGG+8.32
EWSR1-FLI1MA0149.1chr19:45267414-45267432GGAAGGAAGGAAGCAAGC+8.73
Foxd3MA0041.1chr19:45266270-45266282GTTTGTTTGTTT+6.32
ZNF263MA0528.1chr19:45267374-45267395GAAAGAGGGAGAGGAAGGAAG+6.09
ZNF263MA0528.1chr19:45267363-45267384GGGGAAGGGAGGAAAGAGGGA+6.12
ZNF263MA0528.1chr19:45267357-45267378AGGGGAGGGGAAGGGAGGAAA+6.18
ZNF263MA0528.1chr19:45267383-45267404AGAGGAAGGAAGGAAGGAAGG+6.58
ZNF263MA0528.1chr19:45267387-45267408GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:45267391-45267412GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:45267395-45267416GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:45267399-45267420GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:45267403-45267424GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:45267432-45267453GAGGGAGGGAGGGAGGGAGAG+7.43
ZfxMA0146.2chr19:45266677-45266691GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_23197chr19:45267009-45267500Colon_Crypt_1
SE_28964chr19:45267695-45269793Fetal_Intestine_Large
SE_34750chr19:45266161-45269950HeLa
SE_50112chr19:45266843-45267889Sigmoid_Colon
SE_52390chr19:45266220-45266750Small_Intestine
SE_52390chr19:45266904-45267638Small_Intestine
SE_53360chr19:45266833-45267894Spleen
SE_62704chr19:45221152-45271677Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194526693245267832
Number: 3             
IDChromosomeStartEnd
GH19I044764chr194526622145266750
GH19I044763chr194526701045267500
GH19I044765chr194526756845270172
Enhancer Sequence
GTTTGTTTGT TTAATCTGTG GGGGCTTCTC TGGGTCGTCA TGTGAATTGC TGATAGTGAA 60
CATTTAATCC CCATCACTCT GTAATGTAGT TGCATCTGTG GGGCCAGCTG CCTTAACAAC 120
TTCCTGGATG GCATCACTGG GGTCTGTGAA GGGCTGTGTG TGTGCACACA AACACTCATG 180
CACACGCACT TCTGGATGGC CTGTGTGAGC ACTGACTGGG TGACCTGTGT GTGCCTGGCC 240
CGCCTGACTG GGACGTCCAT GCGTCTTTCT GTTTGCAACT ATGTTTCAGT GTTTCTGACC 300
CAGACCCTGT GCTCTGGTAT CTCTGAAGCT GCCAGGCTTG AAGGGCATGT TAATGTCCTG 360
TTGCTGGCCA GGCACGATGG CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCCGAGGCGG 420
GCAGATCACT TGAGGTCAGG AGTTTGAGAC CAGCCTGGCC AACATGGTGA AATCCCGTCT 480
CTGCTAAAAA TACAAAAATT AGCCAGGTGT GGTGGTGTGC ACCTGTAATC CCAGCTACTC 540
AGGAGGCTGA GGCAGGAGAA TAGCTTGAAC CCAGGAGGCA GGGGTTGCAG TGAGCCAAGA 600
TCACGTCACT GCACTCCAGC CTGGGAGACA AAGCGAGAGT CCGTCTCAAA AAAATAAAAA 660
ATAAGAAATA AAAAATCCTG TTGCTGCCAT GCAAACTGCC ACAAACTAGG TGGCTTAACA 720
CAACAGAAAT GTATTCCTTT ACAGTTCTGA AGTCCGGAAG TCCAAAATCA AGGCGTCGGC 780
AGGACCGCAC TCACCAAAAA CTGTAGGGGA GACTCCTTCC TTGCCTCTTC CAGCTTCTGG 840
TAGCCCCAAG CATTCCTCCG CTTCTGGCTG CATCAGTCCA GTCTCTGCCT CTGTCTTCAC 900
ATGATCTTCT CCTTTGTGTG TCCATGTCTT CTTCTCTGTC TCTTATGAGG ACATTTGTCA 960
CTGAGCACAG TGGCTCACAC TTGCAATTCC AGCACTTTGG GGAAGGCAAG GTGGGAGGAT 1020
CACTTGAGGC CAGGAGTTCA AGACCAGCCC AGACAACATA GCAACACCCT GTCTTGAAGG 1080
GAAGGGAAGG GGAGGGGAAG GGAGGAAAGA GGGAGAGGAA GGAAGGAAGG AAGGAAGGAA 1140
GGAAGGAAGG AAGGAAGCAA GCGAGGGAGG GAGGGAGGGA GAGATTATTT CTATGTTTCC 1200
TGGTCAACAT AGTGAGACGC TGTCTCTACA GAAGATCAAA AAATGTGTTG GCTGAGCATG 1260
AGCCTGGTGG TGTGTGCCTG CAGTCCCAGC TACTTAGGAG GCTGAGGTTC AAGCATCACT 1320
TTAGCCCGGG ATGTCAAGGC TGCAGTGAAC TATGATCACG CCACTGCATT CCAGCCTGGG 1380
TGCCAGAGGG AGATCCTGTC TCTTGTTTTG TTTTGTTTTG TTTTGTTTTG TTTTGTTTTG 1440
TTGTTACTAA GTCTCACTCT GCTGCACAGG CTGGAGGAGT GCAGTGGTGC AATCTCTGCT 1500
CACTGCAATC TCCGTCTCCC AGGTTCAAGC AATTCTCCTG CCTCAGCCTC CCAAGTAGCT 1560
GGAATTACAG GCATGCATCA TCATGCCCAG CTAATTTTTA ATTTTATTTA TTTATTTATT 1620
TATTTGAGAT GAAGTCTCGC TCTGTCGCCC AGGCTGGAGT GCAGCGGCGC AATCTCAGCT 1680
CACTACAAGC TCCACCTCCC GGGTTCACGC 1710