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

TagContent
EnhancerAtlas ID
HS047-03748 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr10:16857640-16858970 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7904368chr1016858587hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr10:16858394-16858415AAAATGACACTGAAAGTGACC-6.05
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr101685786816858044
Enhancer Sequence
TCCCAATGTC CCAGCAGAGA AGAGAGACTT CTAGATTAAA AAAGAAAAAA ATCAGTACAA 60
TCCTATGTGA GAGGAGTCAC AAAGCAATAC ACACGACCAC CTTCACAGAG GAGGGAAGGG 120
ATATGTTAGC CTGGTGCAGA CGGATAAGGT TTTACACAGG TGGTGATGTC TAAGCTGACT 180
CTTAGAAGTA AAAGGATTTC AGGTGCAAAC GACTGAGAAA GAGGGAAAAC AGAATTTGTA 240
AAGGCACCAA GATCTGAACG AGTAGGCTCT GGTCCAGGAA GGGCAACAGG TTCAGAATGG 300
CTGGAATGCC AGCTGCATGG AAGGGTAAGG TTGTGTTCAG ATTCAGAAAG GCCTTGTACA 360
TCACGCCAAG AAACCTGGAG CATTACCGTC GATAATGGAC AACCTGGAGA AGTGCGGAGA 420
GGGTTTAAAC CAAAGCCACG TCAGCCTGAA GAACTGCTTT AGCTCACTTA TCACAGGTTT 480
TTCAAATATT AGAATTAGTA GCCAACATCT AAAAATTAGC AAATTTCACA TAAAAATATA 540
GAATCTTGGT TCCTTTAAGA AAATAATCTG GCACATTGGG CCAACATTCC TATGGTGACA 600
TGTGTCTGAG TAGCAGGTGC AGCAGCTGGC CCCTTCAAGT GGGACACCTA TCACCTAGTT 660
CATAACCGCC CCTGACCGCC CTCACTTGGA GGCATGTGAA TCTGCAATCC CTGGTTTTAA 720
GGGAGAGGGT AACACCATAG ACAGGGGTTA CAGGAAAATG ACACTGAAAG TGACCCAGTG 780
ATTAAACTGG GCAGTGAAAC TGAAGGCAAG AGGGCAAGTT AGGAGGATTT CACCACAGCA 840
TGAGGAGGTG ACAAAAGCCT GAACCAAGTT CGGAGAATAA ATACTCAGAA GAATGTAAAG 900
ATTCAAGAAA TGCTTAAAAC GCTCCAGGCA CAAGAATGCT TATTAACCAT GGAACTTTTC 960
TGTGTCATTT GTTCATGGAC AAAGACTGTA TTAGGAGACA GGAAGAAGGA CTCAAAATTA 1020
ATTTTCAATT TATAATTAAA GTGACTATTA AGCAAACTGT GGAAAATCCA CCTCAATGCC 1080
ATACAGCAGA GACAACCGAT GAGGCACAGC TGTCTGTGTG ATTCTCATCG TGGACTCTCA 1140
GGATCGTTTT CCAGGTGGAA CAGAACAAAT CCTACTGCAA ACCCTCTGCG CGAAGCCCCT 1200
GACAAGTGAG GTTTACAAGC AGGGGCTGGG GTCTAAACCA GTACAATCGC TCACAGCAGG 1260
ACCAGCAGTG AATTGGCAAA CTTAGAAAGC CTTCCAGCTC ATCCACGGGA GAGTCCTGCC 1320
CGAGAACTCA 1330