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

TagContent
EnhancerAtlas ID
HS116-20901 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr20:33170640-33172050 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs910873chr2033171772hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr20:33170858-33170873GCAGGTCAAAGGTCA+7.16
Nr2f6MA0677.1chr20:33170859-33170873CAGGTCAAAGGTCA+7.73
PPARGMA0066.1chr20:33170865-33170885AAAGGTCAGGGTGACTCAAT+6.26
RxraMA0512.2chr20:33170859-33170873CAGGTCAAAGGTCA+7.58
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr203317065233171022
chr203317156233171703
chr203317136833171418
Number: 1             
IDChromosomeStartEnd
GH20I034582chr203317078133170950
Enhancer Sequence
ACTTCCAAGC TCTGGTCAGG AGAGAGTTGG GGGACAGAGC TCAATCTCGG TGCCCCTCCG 60
AGAGCTGACC AAGTGCTAAA GGGAAGCCAA CAGGGAGAGG CTGGATCTAT ACCCTCCTCA 120
GCTACATTTC AACCACATGC ACATGGCCTA CTTCTGCACA GTACCTAGAT GCCTAGCCCA 180
TGAAGGTTTT CTTCAGAGAT TAATGACCTT TTTGTCTTGC AGGTCAAAGG TCAGGGTGAC 240
TCAATGGGTA TGAATCTGAG ATGTGCAGAC AAACATGTCC ACACCCAGAA TGCTCCAGTG 300
CTGCTGTGCA GCAAGTGCCT CAGAAACGCA GCTTGGCAAA GGCGTGCAGC CCTGTAGCCT 360
CTAAGAAGCG TCCAGCTATA GCTCAGTGTG AACATCTTCC TAAACACAAT CCACATCACT 420
GGCTTCAGGC TTTTCAGGTA GCTGGTAACA ACGGCAACAT TTCTATGAAA AGGCTGGTGA 480
AAATGCGGTG ACAAAAAAAC AGACTACAGC CTCCTGCAGC ACTGCACAGG GACTGGGGTG 540
GCCTGAAGGG CCCTGTTCCT ACAAAGCTGG CACTGGAAAC AAATCTTGCA GGGGGCAGGA 600
GAGCTTAGGT AGAGCTTCAT ACCCAGGCAG AAGAGAAGAC AGCAGGGAGA GCAGGTCTCT 660
TCATATTTTC TGTCCCCACA ACTGTGTGGG CCTGGCTTAG GTCATAAAAT GGTGACATTA 720
TTGCCTAGCC AGGAGCAATG TGTGGCTTTG CATGCAGACA ATAAAAGCTG CCGGAGAGCT 780
GGCTGCACGG CCAGTGCGGA AAGGTGCCCT GGGATCCCTG CTCCTCTTCA CCCCATGGCT 840
GGGCCTAACC GGAACAAGGA CAGGGAAGGT GGACCACAGA CAGCTGGAGA GCTCAGCTGG 900
GCAAGGCTGC CAGAGTTCCG GAGCCTGCCA GGCCATGGAA GGAGGGTGTT CTGTCAGAAG 960
CCAGGCCAAG GCTGTGTCAT GGGAAGGAAG CATCAGCTTT TGAGATTTTA CAGAATGGGA 1020
ACCACGTGCA TTGGTGCACA GACCATGGAG AATGGCAGGA AGGTTAGGAC AGAGAACTTG 1080
AGCTCTTGAA ACCTAAATCA AACTCTTTCA GGTTCCCCAG ACCATCTAGG CGTATCTGTA 1140
CCTGTCTGTG TCTGTTTTCC CTTATCTGAA GCTAGGATAA TAGAACCATT TCCGGAGGCT 1200
ACTAAAAGCA ATCTCTCCGG AGCTTGGCAT GGTGCAGGGG GATAAGCATA GATTCTGGAG 1260
CCAGACAAAC CTGAGTCTAA ATCCCAGCTC CACTGCTTAC TAGCTGTGTG ACTGGGAAAA 1320
TCATCCCACC TCTCTGAGCA TCGATTTCCT CAACTATAAA ATGGGAGTGA TAAGAATCTA 1380
ACGCCTACCT CCAGGAGTTG CTAGGTTAGG 1410