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

TagContent
EnhancerAtlas ID
HS106-00748 
Organism
Homo sapiens 
Tissue/cell
iPSC 
Coordinate
chr15:65713360-65715130 
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
GACCTCAGTA CAGATCAGGG TGGCTAGTCA TGACTCGACT GGAGTGTCCC CCGGCCTGCT 60
GAGATTTGGA GGACCAGGGC AAGCTGTTGT AGCCACTCAC ACTGCAACCA AGAGACGCCG 120
CAACTCGGTC CCTCGCCTGC TTTGTGCGTT CGGGAGCAGG GAGAGGCCAG GGAAGCTGGG 180
TCCCTCGCGG CAGGTCCTAA AGGTATTGAA TAATGCGCCG GTGCGGTTCC CAGCCCTGAT 240
GCCGTTTAGC TGGGTGACCC TGAGCTCGTT CCAGGAGCCC TAGGAATAGC GGAAGGTGGG 300
GCAGGGGAAC TATTCCTTAA TCCCCTGAGC TCTGGGAAGA CAGACCTCTC TCTGACACTT 360
CCCCGCCCCT TTCACCTGAC AAGCCAGGGC CTCCAGCTCC TCTGGCCCAG CAGCCGAGAC 420
CCAGCCTCGC GGCGGCCTCC AGCTTAATCC GCTGTTGGGG CTGGAAAGGG GCGTGTCTTT 480
GTAGGGACAG AAGGGGTCCG AGGAGTTCCC GGCACTTTCC CACCCGCTGT TTGGTTTTCC 540
TGGAGATGGG CCTGGGGCTG GCCAGGCGGA GGCTCCTTCC CCCCGCCTCC CTCCCACGTG 600
GCCTGGCTGA GTCTCTCTGG AAAGCCGCAG CAGCTGGAGA GAAATCCCCC TCCCCACCCC 660
CACCTCCAAG TCCCTCCCCG ACTCTCCCCG GACACATCCT CAGCTCCCCC CTCCGCGGGG 720
AAGGCAAGAA CTAGGCGAAC AAAGCGGCCA GCCCATCCCC CTCCCAGCCC TGCCACCTAC 780
ACTCCCCATG AGCCGCCCCC AAACGCACAC CGGACAGGAA GCGACAGAGC TGTGGGTGGA 840
AGCCGCAGCC CTAGACACAC ACCCTTGGGG ACTTCGCTAT CCCCTCCCCA GCCCTTTCTC 900
CAGCTTGGAC AACTCTGACT TACCCCGTAC CCACTCCGCA CTGGGCTGCG GACTGGATGA 960
GGCCCTGCTG ACCTCGTCCA CGCTTCCCTG GTCGGTCCCT GGGGGGTGGG GCCGGGGTGA 1020
CACGCGTCCC ATCGTGAGAA CAAGCGCTGG ACATGTCCAC GAAAGCAAAT GGTTTCCTGC 1080
CCCCTCCCCC AGTCCACTGC TGGCCACAGG TTTTGGGGAG CAACACCTCC CTCTACCCCT 1140
CTCTAACCGG CCCCAGGGAC CACACCCACT GGGCAAAGTT GAGTGTTGTT TTATCACCAC 1200
CACCCCCAGT CAAACGGGAT CCATCGCTCT GTCCCCCACT ATGGGCAAGG ACACTTCCCA 1260
AATGCCAAGG CCAAATATTA GCTCAGCCCC ATAAACACAA TTGCACACGC ACCCGACCCA 1320
AATGGAGGTG CAGACACAAC CCCAGTTCCC TCCTCTTTTA CACACACTCT CAACCCAAGA 1380
CACGCGCAGG CAAGGCAGAG CCCGCCCCGC GAAAGCCACC GACACCGCAG CTACCCGCCC 1440
CGCCGATGCC ACGCCGCGAC CATGGCACGC ACTGCGGACA CGACAGGAGC ACTCCCAACA 1500
CACACACACA CACACACACA CACACACACA CACACGACTC CAGACTCTGC GAACCAAAGG 1560
CACACACCCA CTGCGGACAA GCACGCCCCA CAAACGCCCC CCGGCCGCAG CTCGCAGACC 1620
CCCGCGCAGG CATCGCGGGC ACCTGGACGC GCAGCCCCCG CACTTGCTCG GGACTCCGGC 1680
TTGAGCCAGC CCCGCAGCCC GATGCAGACC AGGGCGCGGG CGCACCAGCA CTCCGCAGTC 1740
GCTCCTGCCT CTCCGGGCGC CCGCCCTTAC 1770