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

TagContent
EnhancerAtlas ID
HS184-18539 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr20:55309840-55311010 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs34871495chr2055310283hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr20:55310917-55310937CCCCACCCCCACCCCCACCC+6.27
RREB1MA0073.1chr20:55310918-55310938CCCACCCCCACCCCCACCCC+6.27
RREB1MA0073.1chr20:55310923-55310943CCCCACCCCCACCCCCACCA+6.27
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr205531020055310505
Number: 2             
IDChromosomeStartEnd
GH20I056736chr205530977355309850
GH20I056734chr205530998355310678
Enhancer Sequence
AAACCCAAAA AACTGATGGA GGCACTTTCT TAAGCAGATT GGAGGCCCTG CACCCTGCTA 60
GGGGCTGGGT CCCCACCCTG GAAGCCTATA TTTAGATATC TGAGAGTGAA ACAGGAGGGA 120
AAGAAACAAA ATGAAGAAAA CTTCTGTAAG CCTCAGTTTC CTCGTGCAAA ATGTGGACGT 180
TAATAGTATC TCCTTACCTC GGGGTCACCA CGGTATTGGA TAAAATAATG CCAGTAAAAG 240
GTGTCCCAGT ATCAGAGAAG ATGGCCATTA CTCAAAGGCT TGCTCTAGCA AATGTCAAGC 300
TACAGACAGA AATCAGCGCT CTCAAGGAGA GCTTGAGGGT GAGATTTTGG TCTAGATTTG 360
GGCATGGCAG TGGCAGTCGG GAGAGGCTTC CCTGGGGAGG CAGCCAGGCC TGCAAACGGT 420
GTTTATCGTT CTCTCCATCT GGCATTAGGG CCAGAGCACT ACTGTCTCTC TGTTCCCCCA 480
ACACGACGCG CTGCCAGCAC CCACACTGCT GCAGAGCCTT AGCACAGGCT GCTTGCTCCG 540
CTGGATCACA CCCAAACCAT GGCCTGGCTG GCTCCTTGTT GACTTTCAAT TCTGAGATGA 600
ATGATCATCT CCCTGGAAAA GGCTCTGCCA CTCTCCAATG ACCCAGCTCT GGTTTATCTT 660
CACCGTGCTG ATCGCCCCTG CAATCTGTTT GCTTTCAGCT CTTGGACCTG TTCTTCCCTA 720
CCCACCCAGG TGCGCTTGGT GCTGTGTGCA CAGTAGGTGC TCGGTCAATA TTTGTCCAGG 780
GCATAACACG CCTTCCAGCA GTGTGGCTCC AGCTCCGAGG GCATATTCAT CATCGGGGGA 840
TCTTGTTAGA ATCAAGGGTC CAGTTCAGTA GGTCTGGAGT GGGGCCCAGG AGTCTAAGTG 900
TCTGAGAAGC TTCCAGGTAT TGTGATGCTG CAGGTAGGTG GGCCGTGCTT TGGGGTTCAA 960
GAGTGTGTGA ATGGGACAGC TGCGACCTGG GGCGTCAACA GAGGGAGGGG CTGGTTGAAA 1020
CAGGGAGGGG CTTCATTGAG GAGGAGACCC TGATATTTAA GTAATGGAAT TTGTCTCCCC 1080
CACCCCCACC CCCACCCCCA CCATCCCTTC ATCCCTGCTG CCATTATTTC TCAGCCACGT 1140
TATTTTTTTT TTTTGAGACA CAGTCTCGCT 1170