Tag | Content |
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EnhancerAtlas ID | HS108-14638 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:11458330-11459590 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX5 | MA0510.2 | chr16:11458583-11458599 | GGTTGCTAAGGAAACC | - | 6.07 | TFAP2A | MA0003.3 | chr16:11459170-11459181 | CGCCTCAGGCT | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_39207 | chr16:11457776-11459255 | IMR90 | SE_44615 | chr16:11452928-11459306 | NHDF-Ad | SE_68391 | chr16:11438909-11459249 | TC32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 11459142 | 11459235 | chr16 | 11459383 | 11459513 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I011353 | chr16 | 11447820 | 11459775 |
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Enhancer Sequence | GTCATTGCCA GGTGACCTTG TCAACCATGG GTGTACAAGG ACAAACCAAA TCCGGGTGAA 60 AGAATTTGTG CCTTGTTTTC TTTGCCTTTG ACCTTCAGCC CCGTGCATTC CTGCAAATGC 120 ATTGCCCCTG GTAAACCTTA AGAAGACCTT AACTTTTCTG TTTTAAGTGA GATTTCCAAG 180 TTAATTTAAG TTGTGTGGAA CAGGACACTC CCTTTACTGG AGAGCAATTG GTATCTGAAG 240 AGAATGAGAT AGAGGTTGCT AAGGAAACCC TTGTTTGCAA TGTTTGGTTT ACATAAATTA 300 TTGGTGAATA AGAAAAATAA GTTTATTCCT TCTTCCAGAT GGTAAACTGG AAGGGAAGCA 360 TGTTACTGGG TAAAGTGAGT CATGGGCCGT GGGAGGCTCA GATGGAAAAG GGCTCTGGGA 420 TGCCTCTCTC TCTCTCTCTT TACTTGGGAC CCCTTTCTAA TTTACCTACC AGGCCTCAAA 480 AGACAAAGCC CTCTAATCTG TTTAGGCAGG AACAGATAAA ATTCCTCTGG GTGGATGGGT 540 AGGGGAGGGA AGGAGGAAGT TTGCAGAAAC TGAAAGAGAA CTTTTTTGGG GGGAGAGGGA 600 GAAATCTCTT GTTTAATTAC AAAACCAAAA TATCATTTGC AATGCCTTCC TTCTCCTACT 660 AGTCTTAAGG AATTGATAAG TAATTCACAT ACCACAAAAT GCAGCACTTT AAAGTGTACC 720 ATTCTCTGAT GTTTTTTGTT TGTTTTTGAG ATGGAGTCTC GCTCTGTCAC CCAGACTGGA 780 GTACAGTGGC ACGATCTCGG CTCACTGCAA CCTGCGCCTC CTGGATTCAA GCCATTTTTC 840 CGCCTCAGGC TCCCGAGTAG CTGGGGTTAT AGGCACCCGG CATCATGCCT GGCTAAGTTT 900 TGTATTTTTT GTAGAGATGA GGTTTCACCA TGTTGGGCAG GCTGGTCTTG AACTCCTGAC 960 TTCAGGTGAT CTGCCTGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCA TGAACTACCG 1020 TGCCTGGCCT TTCTCTGGTG TTTAGTGTAT ACACAGTGGT ACAACCATCA CCACTACTAA 1080 TTCGAGAACA CTTCATCACC CTAAAAGAAA TGCCATACCC ATTAACAGTC AATCCCACAA 1140 TCCTCCCATC CCCCTCAGCT CTTGCAATCA TGAATGTACT TTCTGTCTAT ATGAATTTGT 1200 CTGTTTTGGA CATTTCCTTC CAATGTAATC ATACAATATG TAGCATTTCG TGTCTGGCTT 1260
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