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

TagContent
EnhancerAtlas ID
HS182-10270 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr18:9173260-9175580 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs144675973chr189173626hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr18:9174642-9174653CCACACCCTGC+6.62
NFE2L1MA0089.2chr18:9173840-9173855AAGGCTGAGTCATTC-6.14
POU2F2MA0507.1chr18:9175286-9175299ATATGCAAATTCT-6
RREB1MA0073.1chr18:9173603-9173623GGTGGGGTGGTGGGGGGGGG-7.36
ZNF740MA0753.2chr18:9173614-9173627GGGGGGGGGGTAG-6.13
ZNF740MA0753.2chr18:9173612-9173625GTGGGGGGGGGGT-6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr1891735829173632
chr1891738789174287
chr1891747619175238
chr1891754429175488
Number: 1             
IDChromosomeStartEnd
GH18I009173chr1891739029174798
Enhancer Sequence
CTTCACAATG TTGGCCAGGC TGGTCTCAAA CTTCTGATCT CAGGTGATCC GCCCTCCTCG 60
GCCTCCCAAA GTCTGAGATT ACAGGCATGA GCCACCACGC CTGGCCAGTT GCTGACCTTT 120
AAATGGGGTT TTTGTGGTGT CTTTTTTGTT GATACTCTTG TTGTTGTTTT CTGTTTTTCT 180
TTTAACAGTC AGTGCACTTT TCCATAGGGC TGCTGTAGTT TGCTGGGGGA TTGCTGCAGA 240
CCCTAGTTGT CTTGGTCTTT CCTTTACCTG TAGGTATATC ACCAGTGAAG GCTGTGAAAC 300
AGCTAAGATG GCAGTCTGCT CCTTCCCTTG GGAGCTCCAT CCCGGTGGGG TGGTGGGGGG 360
GGGGTAGGGG GGGCAGTACT GACCTGTTGC CAGCCTGGAT GCTGCTGTAG AAGGTGTCTG 420
GAGATCCCCG TTAGGAGGTC TCACCCAATC AGGAGGGACA GGATCAGGGA CCTGCTTAAA 480
GATGCAGTCT GGTTGCTTTT TGGTAGATCA GGTGTGCTGA ATTGGGGGTA ACCGTTCCTT 540
GCCCAGACTG CCTGGACTCT CCAGAGCCAG CCCGCTTAGA AAGGCTGAGT CATTCGTGTA 600
CCCTAAAACT TAAAGTATAA AAAAATAATA AGAAGAAGAA AGGCTTAGTC AACTGAACCG 660
CAGAGACATT GGGCACTCCT CCCCCTAGGG GCTTGTCCCA GGGAGAGATC AGAGTACTGT 720
TCATATAACC TTGGCTGGAG TTGCTGAAAT TCCCTCAGGG AGGCCCCACC CAGTGAGGAG 780
GGATGGATTG GGGTCCCACT TAAAAGAGCA GTCTGGCCAC GATCTGGCAC AGCAGCTGTG 840
CTGCCCTGTG AGGGACTCCT CCTCATCAGG ACCACCTGGA TTCTTGGGAG CAGGCTAGAA 900
CAGCTGGGTC AACTGAACTG CAGAAATGGC AGCCGCCCCT CCCCCTGAAA ACTCATCCAT 960
TTTAGGCAGT CTCTAGCCTG TTGCACTGGC TGGCTAGAAT TCAAAGCCAG TGGGTTGAGG 1020
TGCCATGGAA GTGAGGCCCG CAGAATGACA CTGCTTGGTT CCCAGGATTC AGCCCTCTTC 1080
CTAGGGGAGG ATACGGATGG ATTTCTCACC TTGTTGGGAT TCCCAAGGGT GGAGTCTGTA 1140
AAACTCCTGG GTTTACGTGT GAGCCTGAGC AACTGCTCTG CCAAGACTCC GCACAGCTCT 1200
GTATGTTGGA CCTAAGTAAG GCCCTGGTGG CCTGGGTTCA TGAGGGGATC TCCTGATCCA 1260
TGGTTGCAAA GATCCGTAGG AGAAGTGTGG TTTCCTGAGT GGGGTTACAC AATCACTCAC 1320
TGCTTCCCTT GGCTGGGGGT GGGGGTTCCT TTGGCTCCCC AGTGCTCCTG GGTGGGCCAT 1380
TGCCACACCC TGCTTTTTTT GTTGTCTGTG GGTCATGCCA TCCTCCTAAT CAGTCCCAGT 1440
GTGAGAACCT GGACATTTCA TTTGAAGGTG CTGAATTCAC TTGCTGTTGT CATTCTTCTC 1500
TATGAGAGCC ATCTTGTTTC TAATCGGCTA TCTTGGCCCC TCCTGCCCCC TTCTTGTCTT 1560
ACAGGTGGAA ACTGAGGAAT AATCCCAGTG CTTTGTGAAA CTGCTATGAA GAATATTCAA 1620
GTCAGACTTA AGTTGGAAGA TAGTGACTAG AGCAAACAGA CCAAAGCATT TATTTATTTA 1680
TTTATTTATT TATTTAATTT GTTCATTCCT GAGACAGAGT CTTGCTTTGT TGCCCGGGCT 1740
GGAGTGCAGT GGTGTGATCT CGACTCACTG CAACCTCCAC CACCCAGATT CAAGCAACTC 1800
TCCTGCCTAA GCCTCCAGAG TAGCTGGGAA TACAGGCGTG CGTCACCACT CCTGCCTAAT 1860
TTTTTGTATG ACCAAAGCAT TTAAAGCATT GATTCTGAGG GCCTGGAACT CACTAAATGC 1920
TGCCAGACTC TAAAGTGATC TCAAAATAGA CTTTCTGTAG TTGGAATACT TCTGTAGATA 1980
TTCACTTGTA TTATACATGT GCAGTCTCCA TGTTTGTAGC ATTCAGATAT GCAAATTCTA 2040
TTATTTCTGT TCCCCATAGT CCTCTAGGCC ACATTGGCAA CTAGAGGTGT TTTTTTCTCT 2100
CAGCCCTATC TTCTAAATAG TCTGAGTTGT CTTTCTCTGT TATTGGATTT TCTCCCTGAT 2160
TCTCCCTCCT TTTGTCAGTG TTCAGTAGTT TTTCGTCCAC AGAAATGGTC CCAAGGCTTC 2220
TTTCCTTCTT GATCACTTGA TCAGTTTTTC AAAGGCTCCT CTTTTTTTTT TTTTTTTTTT 2280
TTTTTTTTTG AGACAGTCTC TGTCATGCAG GCTGGAGTGC 2320