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

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EnhancerAtlas ID
HS002-04905 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr19:19692530-19693960 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7252981chr1919692579hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr19:19693910-19693925GAGGTCAGGAGTTCA+6.22
PLAG1MA0163.1chr19:19693353-19693367CCCCTTTGGGCCCC-7.31
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191969314819693782
Enhancer Sequence
CCCAAGAATG CCAGCCCAGG GGTGTCAGGA AGGCTGCGGG AACCCAGGTC ATGCGGTGCT 60
GCCATTGGCT TTGGGAGCTG AGGGACTGGA TAAGGTTATT GGCCAAGGAA GGTGTTCCTG 120
CCACGATGCA AGGTGACAGT GTGAGAATAG GTGGGGGCTT CCAAGTGGCT GGGTGGTGCT 180
CTGAGCAGCA GGAGACGAGA CTGGCTGTGA GAGGCCTATG GAGGAAGTGG TACCGCCTGA 240
TTCCCCAGGA GAGTGCCCTG GGATGTGAAG GACATCGTGG GGTGGCCCCA GCAGGAGGCT 300
GGGGAGCCCA ACACAGTGAA GGCAGAAGGC CAGCAGGACT CTTCCATGAG AACCCAAGGC 360
CCCCTACCTT TGGGATCTGG CCTCATTTGC TCCTGGCACC TCCTCCCACC CCCCAAATCC 420
TGCTGCTGCA CACTCCTCTC ACCTCTCAGC TCCAATCTAG CTTCCCAGTG ATACGGGAGT 480
GGGGCAAGGA AGTGCTGGGT AGAGAAGGGC GGGGTCCCTG GCGAGGGCTC CACCCTCGGC 540
CCTGTGCCCT CGGACCTAAG TGAGAACAAG CATTTCTGTT TTTGTGGCCA AAAGGTTGCC 600
TTTTGGCCTG CCACGCCCCA CATCTTGTGC CCAAATAAGC CTGAGACCTT AAGCAGACAC 660
ACACAAGCAG CTGGAAGTCG AGAGGAACAC ACCAGCAGAA GAACACACCA ATAGACACTG 720
GCGGGCCATT GATGGTGGAA CAATGCAGAC ACCAAGGGAA ATCCAGGAGA GCCCAGTCAC 780
TGAGCGGCCC AACTCCAGGG CAAAACCACC TTCCCAATCC AACCCCCTTT GGGCCCCCCA 840
TCCATCTGCT GAGAGCTACC TACACCACTC AGTAAAACCC TGTACTCATT CTCCATGCCC 900
ACATGTGATC CGATTTTTCC AGTACACTAA GGCAAGAACC CCAGAATATA GAAAGCCCTT 960
TGTCCTTGAG ATAGGGCAGA GGGTCTAACT GAGCTGATTA ACACAAGAAG CCTGCTTCTC 1020
TTTCAGCTAA GCTGAAAGAG CACACTGTAA CGCATGCCCA CTGGGGCTTT GGGAGCTATA 1080
AACACAACCC TAAGACGCTG CGCTGCTGCT GTGGGGTTGG AGACCACGTT CCCCCCACCT 1140
GTCTGACTGC ATGCTCCCCC TTAGGGGTTT GAGCTGTGGG GCACCGAAGA AGTGAGCCAC 1200
ATCCGTCACA CACCCTGCAA GGGGGAAAAG GGAACACTCC TGTTTCACCC GGGCTCCGGG 1260
AACACCAAGC TCAGGCCTGC GTCATGAACT CTTTCCCAGC AAGAGAGCGG AGGTGGCCAG 1320
GCGCGGTGGC TCATGCCTGT AATCCCAGCA CTTTGGGAGG CTGAGGTAGG TGGATCACCT 1380
GAGGTCAGGA GTTCAAGACC AACCTGACCA ACATGGCGAA ACCCCGTCTT 1430