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

TagContent
EnhancerAtlas ID
HS091-43723 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr7:44961000-44962400 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs55738054chr744961337hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr7:44961876-44961895TCGCGCCCCCTGGTGGCCG-8.35
RREB1MA0073.1chr7:44961724-44961744TGGTTGGGGGTGGTGGTGGG-6.67
RREB1MA0073.1chr7:44961727-44961747TTGGGGGTGGTGGTGGGGGG-7.18
SOX10MA0442.2chr7:44961151-44961162AAAACAAAGGA+6.32
Sox3MA0514.1chr7:44961151-44961161AAAACAAAGG-6.02
ZNF263MA0528.1chr7:44961665-44961686CCCTCCTCCCCTTCCTCACCA-6.75
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr74496121244962169
Number: 4             
IDChromosomeStartEnd
GH07I044921chr74496130144961450
GH07I044923chr74496159944961800
GH07I044924chr74496180144961970
GH07I044922chr74496199944962199
Enhancer Sequence
AGCGATTCTG GAGGTTGAGG CAGGAGAATC ACTTGAACCT GGGAGGCAGC AGTTGCAGTG 60
ACCTGAGATC ATGCCACTGC TTTCCAGCAT GGACAGCAGA GCAAGACTCC ATCTATAAGT 120
AAATAAATAA ATAAAATTCC CTAGGTGCTT AAAAACAAAG GAAGAGGAAA AAAAAGGAGG 180
TGCATCTAAC ATCTAGGAAG AGCACCTGGG GGAGCACCTA CTGGGAGCAC CTGAAGGAGC 240
AACTCAAGGG CCACTGGCAG GAACCTCCGG GAAGCGCAGA AGGCATGTGT GGGGAGAGAT 300
TGGTGGGGGT TGGGTGTTCT TACCTACTGA ATGGGCGGGC TAGATCAAGA GGTGACAACC 360
TGGAAGAGAA ATGGGGCTAG AGACAGGCTG GCTGTAAACC AGTGGTTGTC GAGGAGATAG 420
CATCAGTGAG GGAGGTGCCC CAGTGGGAGA GCCGCCCTGA AAAGGGAGGA GGGTGTCTCT 480
CCACTGTTGA GCCAGAGCCA CAAAGAGGGT TGACTCTGCC ATAGAGCGGC CTTTCTTCCC 540
AGCTATTATG TCGGCTCTGC AGGGACCCTC ACACTTGATG AGTCAAGGGG CTTGTGCCTT 600
ACTGAGCAGC CAGAGGGATC CCTCTCTGAG ACCCTCAGAC CTGCTCCTTG CCTGACCAGT 660
GCCAGCCCTC CTCCCCTTCC TCACCAGGGG ATGGCTGAAG CATGGAAAAG TGGCCGGCAG 720
CAGATGGTTG GGGGTGGTGG TGGGGGGCAT GGGGACTCAA CGCCCTGGGT TGCTGAGTCC 780
TGTGAGACCT GTGGCCCCGG GACACCCCAC CCCAGGCCTG GGCTCTCAGC AAGAATGCCA 840
TGTGGAGCCT GTCAACTAGC CCGTCAACTA GCACTCTCGC GCCCCCTGGT GGCCGTCCCT 900
GATGAGGTGG GTATAGGACA TGGTCCCAGT GAGAACTTGT GGCAATCCAC AGTTCATGCC 960
TACGTTCATT CATTCATTCA TTCTTGAAAT ATTTGGGGAG TACCTGCAGG CCTCCGAAGC 1020
TCTATGCTGT CCACTCTGGC ACCCACACGT GCTCTGAGCA CTTGAAGTGC AGCGAGTCCA 1080
CTGGAGAAGT ACAGTAAGTG TAAAGAGTAC ACTGGCCGTC AAAGACATAG TGCACACAAT 1140
GTAAAATGTA GTATCGATCA TTTTCATATT GATGATACAT TGAAATTATA ATGTTTTAGA 1200
TCAACCATTT TAAATAAAAT ATGATTACAA TCAATTTCAC CTGTTTCTTT TTTACCGAGA 1260
CCAGCTGGGT CGGGGAGACC CTAACCTAGT GGTGCTAGAG GAATTAAAGA CACACACACA 1320
GAAATATAGA GGTGTAAAGT GGGAAATCAG GGGTCTCACA GCCTTCAGAG CTGAGAGCCC 1380
CGAACAGAGA TTTACCCACA 1400