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

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EnhancerAtlas ID
HS119-00363 
Organism
Homo sapiens 
Tissue/cell
LNCaP-1F5 
Coordinate
chr2:3473600-3474550 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs35067331chr23474085hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr2:3474048-3474065AAGAACACCCTGTTCCA+6.14
ArMA0007.3chr2:3474048-3474065AAGAACACCCTGTTCCA-6.44
NFAT5MA0606.1chr2:3474538-3474548ATTTTCCATT+6.02
NFATC1MA0624.1chr2:3474538-3474548ATTTTCCATT+6.02
NFATC3MA0625.1chr2:3474538-3474548ATTTTCCATT+6.02
NR3C1MA0113.3chr2:3474048-3474065AAGAACACCCTGTTCCA-6.01
NR3C2MA0727.1chr2:3474048-3474065AAGAACACCCTGTTCCA-6.01
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_01750chr2:3467163-3477139Aorta
SE_41159chr2:3468278-3477371Left_Ventricle
SE_49115chr2:3468345-3477656Right_Atrium
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr234737163473801
chr234738933474499
Number: 1             
IDChromosomeStartEnd
GH02I003469chr234730203475997
Enhancer Sequence
AGCAGCAGTC ATGAGCATCC CTTACAAATC ACATTGTAAC ATCTGAAGTC ATGTAACACA 60
AAGCTAAACG CGCGTGGAAT AAGATTGATT TCGTTTCTCT GAGATTAGTT TCTACTCTTA 120
TGTGCATGGA GATACAAGGG AGGCTCGGCA TTTTCTACAA TCTTGAATGT TATCTCCAGA 180
CCAGGGAGGA TTTGGGTTTC ATCAGCATTG AAGGTGGGAG ATGAGGTGGG CATCGCGTCG 240
ATGCTGAGTC TCGGGGAGAA AGCTAGGAAA TGTCCCCAGC AGGTAGGGAA ACGCTTGGCA 300
AAGCACAAAG GCAGAGGGAC CCACATAGCT GGGCCCATTC TGCTCACGCC CTGGCACTAC 360
TGCAAGAACT GTGGTTTTCC GGGTCAACCC TAGCGAGGAG GGAGCACAAG CAGAGCTTCT 420
CTGCGGAGAA GGCAGATTTC CAGCTCCTAA GAACACCCTG TTCCACAAGG AAGCTGACGT 480
GCCCCTCCCC AGGGACCCAC GCCAAAAGGC CATTCTTCCA GGCCAGCGTC CCAGGGCGCT 540
GCTGTGCGTG GTTCGCAGCC CCGGCAAACG ATGGCCTGCA CTGCGTGCTG TCCGCCCTGT 600
TCCTGCTGGA CTCTCTGCAC TGTGTCCTGA TCACCCTCTC AGCTGATAGT GGGCACTGCA 660
GTGTGAATCT TCTCATGGAC AACAGACCAA TCCTGCCTCC ACCAGTGCCG TCGCCAAATC 720
AGTAACACAG AGCAACCTCA AACATTTCTG AATGTTTAGG TCATCTAATA CTTGGCAAAA 780
GAGTGGGCCG AACACCTCCA CCCTCAGCTT TCTCTTCTGT TTGTGTGTGA GTGTGTGTAG 840
CAGAGTCTGA GAAAGATACA TACAGCCACC TTCCTTTTCT GAGCTTGGGA AAATTTGAAC 900
AAGAGCACTG AAATGCAAAC ACTAATCAAA AAGGAAGTAT TTTCCATTTT 950