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

TagContent
EnhancerAtlas ID
HS034-03327 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr10:43817850-43818820 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10899789chr1043817859hg19
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr10:43818453-43818464GGGGGCGGGGC-6.02
KLF5MA0599.1chr10:43818360-43818370GGGGCGGGGC-6.02
KLF5MA0599.1chr10:43818454-43818464GGGGCGGGGC-6.02
RFX1MA0509.2chr10:43818330-43818346CGTCACCATGGCAACA-6.93
RFX1MA0509.2chr10:43818330-43818346CGTCACCATGGCAACA+6.94
RFX2MA0600.2chr10:43818330-43818346CGTCACCATGGCAACA+6.87
RFX2MA0600.2chr10:43818330-43818346CGTCACCATGGCAACA-7.03
RFX5MA0510.2chr10:43818330-43818346CGTCACCATGGCAACA+6.71
RFX5MA0510.2chr10:43818330-43818346CGTCACCATGGCAACA-6.83
SP1MA0079.4chr10:43818452-43818467AGGGGGCGGGGCTGA-6.06
SP2MA0516.2chr10:43818451-43818468GAGGGGGCGGGGCTGAG-7.79
SP4MA0685.1chr10:43818450-43818467GGAGGGGGCGGGGCTGA-6.47
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr104381818143818800
Number: 1             
IDChromosomeStartEnd
GH10I043322chr104381776243819102
Enhancer Sequence
CCCCACGTCA TTTACCAAGG CCACTTGCCC ATACCACAGA CAGAGAGTCC TTGGTTTCTG 60
GTCCTGCCAG TCAGAATTGG GCGGAACTGC CAAGTTGGCC CAACCCTACT CCAATCCCTG 120
ACAAAGGGAG CGGCCTTCAG GAGGCTCGGC TCTCTGTGCA CTTTGCTCAA GATACCTGAA 180
GAATGATTAC TTTGAGGAAG AAAGGAAGAC TTTTAGGAAA GAAGCGACTT TGTTTTCGCG 240
GTCAAGGAGC GAAGGCCCCA AGAGACCAAG GTAGACGCTG AAGGAATCCG GGAAGATGAC 300
AGAAGCGGTG AAGAGACGCG AGGTGGGGCC AAAATCTTCA CTAACCAACA AGGAGGGCTG 360
CGGGGGCTTT GGAGGGCCTC TTTTCTCGCA ACCGTGGCCC CTCCGCCCCT CACCTGCCCC 420
TTGAGTGTCT GTGCAGGGGT CTCACACGCG AGCTTGGCTA CTCAGACCAA GCCGGTTTAC 480
CGTCACCATG GCAACAGCGC GTCCTGGGCT GGGGCGGGGC CAGACTGCCA GTGCCTTTGT 540
GGCGCATTAG GAGCTAAGCC AGTGATTGGC CATCTGGGCG CGGGGCGGGC TGAGTCAGTT 600
GGAGGGGGCG GGGCTGAGGC TCCGGTGAAC GCCGTAGGCC CGGGCTGGGC CGAGGGAGAT 660
GATGGATGCC GCTTCTTGCC ACTCCCCGGG GGCACCACAG AGAGCGGGGA GCCTGCAGAG 720
AGCAGGGACA GCGGCTTCAA ACGCACTGTT TCCGGGCAAT GTCACTAATA CCAAAGTCAT 780
GCCTCCCACT GGACACTCCT GGGCTCCCAT CCTTCCTACC AAGAAACTTT CTCTGTGAAA 840
CCCACGAAAC AGCTAGAAAT GGAGCCCAAA AGATAGCCAG GATAACAGAC CACAGAGAGG 900
ATCAAGGCCC AGCAGGACCT GGCGACTCTA ACGCTCTGGC ACTAGGGTGT CTAGAATGGG 960
AAGCCCCCAA 970