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

TagContent
EnhancerAtlas ID
HS007-05747 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr15:65713330-65715130 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs28665840chr1565713813hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gfi1bMA0483.1chr15:65713416-65713427TGCTGAGATTT-6.32
KLF13MA0657.1chr15:65713821-65713839TGGAAAGGGGCGTGTCTT-6.47
KLF14MA0740.1chr15:65713824-65713838AAAGGGGCGTGTCT-6.04
SP4MA0685.1chr15:65713823-65713840GAAAGGGGCGTGTCTTT-6.15
ZNF263MA0528.1chr15:65714006-65714027CCCCTCCCCACCCCCACCTCC-6.36
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_29872chr15:65705313-65716673Fetal_Muscle
SE_33345chr15:65713095-65715216H1
SE_37505chr15:65711690-65716694HSMMtube
SE_69036chr15:65713044-65716115H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr156571378165714189
Enhancer Sequence
GCTCCATAAA TATTTGTTGA ACGAATGAAT GACCTCAGTA CAGATCAGGG TGGCTAGTCA 60
TGACTCGACT GGAGTGTCCC CCGGCCTGCT GAGATTTGGA GGACCAGGGC AAGCTGTTGT 120
AGCCACTCAC ACTGCAACCA AGAGACGCCG CAACTCGGTC CCTCGCCTGC TTTGTGCGTT 180
CGGGAGCAGG GAGAGGCCAG GGAAGCTGGG TCCCTCGCGG CAGGTCCTAA AGGTATTGAA 240
TAATGCGCCG GTGCGGTTCC CAGCCCTGAT GCCGTTTAGC TGGGTGACCC TGAGCTCGTT 300
CCAGGAGCCC TAGGAATAGC GGAAGGTGGG GCAGGGGAAC TATTCCTTAA TCCCCTGAGC 360
TCTGGGAAGA CAGACCTCTC TCTGACACTT CCCCGCCCCT TTCACCTGAC AAGCCAGGGC 420
CTCCAGCTCC TCTGGCCCAG CAGCCGAGAC CCAGCCTCGC GGCGGCCTCC AGCTTAATCC 480
GCTGTTGGGG CTGGAAAGGG GCGTGTCTTT GTAGGGACAG AAGGGGTCCG AGGAGTTCCC 540
GGCACTTTCC CACCCGCTGT TTGGTTTTCC TGGAGATGGG CCTGGGGCTG GCCAGGCGGA 600
GGCTCCTTCC CCCCGCCTCC CTCCCACGTG GCCTGGCTGA GTCTCTCTGG AAAGCCGCAG 660
CAGCTGGAGA GAAATCCCCC TCCCCACCCC CACCTCCAAG TCCCTCCCCG ACTCTCCCCG 720
GACACATCCT CAGCTCCCCC CTCCGCGGGG AAGGCAAGAA CTAGGCGAAC AAAGCGGCCA 780
GCCCATCCCC CTCCCAGCCC TGCCACCTAC ACTCCCCATG AGCCGCCCCC AAACGCACAC 840
CGGACAGGAA GCGACAGAGC TGTGGGTGGA AGCCGCAGCC CTAGACACAC ACCCTTGGGG 900
ACTTCGCTAT CCCCTCCCCA GCCCTTTCTC CAGCTTGGAC AACTCTGACT TACCCCGTAC 960
CCACTCCGCA CTGGGCTGCG GACTGGATGA GGCCCTGCTG ACCTCGTCCA CGCTTCCCTG 1020
GTCGGTCCCT GGGGGGTGGG GCCGGGGTGA CACGCGTCCC ATCGTGAGAA CAAGCGCTGG 1080
ACATGTCCAC GAAAGCAAAT GGTTTCCTGC CCCCTCCCCC AGTCCACTGC TGGCCACAGG 1140
TTTTGGGGAG CAACACCTCC CTCTACCCCT CTCTAACCGG CCCCAGGGAC CACACCCACT 1200
GGGCAAAGTT GAGTGTTGTT TTATCACCAC CACCCCCAGT CAAACGGGAT CCATCGCTCT 1260
GTCCCCCACT ATGGGCAAGG ACACTTCCCA AATGCCAAGG CCAAATATTA GCTCAGCCCC 1320
ATAAACACAA TTGCACACGC ACCCGACCCA AATGGAGGTG CAGACACAAC CCCAGTTCCC 1380
TCCTCTTTTA CACACACTCT CAACCCAAGA CACGCGCAGG CAAGGCAGAG CCCGCCCCGC 1440
GAAAGCCACC GACACCGCAG CTACCCGCCC CGCCGATGCC ACGCCGCGAC CATGGCACGC 1500
ACTGCGGACA CGACAGGAGC ACTCCCAACA CACACACACA CACACACACA CACACACACA 1560
CACACGACTC CAGACTCTGC GAACCAAAGG CACACACCCA CTGCGGACAA GCACGCCCCA 1620
CAAACGCCCC CCGGCCGCAG CTCGCAGACC CCCGCGCAGG CATCGCGGGC ACCTGGACGC 1680
GCAGCCCCCG CACTTGCTCG GGACTCCGGC TTGAGCCAGC CCCGCAGCCC GATGCAGACC 1740
AGGGCGCGGG CGCACCAGCA CTCCGCAGTC GCTCCTGCCT CTCCGGGCGC CCGCCCTTAC 1800