Tag | Content |
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EnhancerAtlas ID | HS108-14442 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:2976700-2977600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:2977223-2977242 | CAGCACCACCTAGTGGACA | - | 6.74 | NKX2-5 | MA0063.2 | chr16:2977094-2977104 | CTCAAGTGGT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 2976927 | 2977585 | chr16 | 2976800 | 2977200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I002926 | chr16 | 2976509 | 2978253 |
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Enhancer Sequence | TATTGTAGAA TTAATGGCCT ATGAAAATGC AAATCCGGAA TGTCAATTGG CCATAAAGCC 60 ATGTTGACTA CAATCAATTA CAGGAGGTAA CATATCCTGA ATCATCAAAA TTGGGGGGAA 120 AAGTGGGGCC ATCAGAGTCT AAACCACAAT GGCCAACTCC TCCTCCCGTG GTTCAGATAC 180 CTGTAACATT ACAACCTCAA ATGCAGGTTA GACAAGTACA AACCCCAAGA GAATATCAAA 240 TAGAAAAGGA TAGTCTCTAT CTCGGCAATG CCAATCCAGA TACAGTATCC ACAATATCAG 300 CCAGTAGAAA ATAAAACCCA ACCGCCATTA GCTTATCAAT ACTGGCTGCC AGCCGAGCTT 360 CAGTATTGGC TGCCTCCAGA GGTCCAATAC AGACCTCAAG TGGTGTGTGC CATGCCAAAT 420 TGCACGGCAT CGTACAAGCA ACCCATGGCG GTGGTGTTTA ATACGTCAGC ACCACAGGGC 480 GCGGCGCTGT GTCCTCAGCC GCCCACTATG AGACTTAATC CAACAGCACC ACCTAGTGGA 540 CAAGGTAGCA CACTGCACGC GATCATTGAT GAAGCTAGAA AACAGGGAGA TCTTGAGGCG 600 TGGCAGTTCC TGGTAATTTT ACAATCGGTA CCGGCCGGGG AAGGGGCTCC AGCAGGAGCA 660 CCTGCGGTGG CTAATGCTAG ATATGAACGC TTCACCATGA AAATGTTAAA AGACATGAAG 720 GAAGGAGTTA AACAATATGG ACCCAACTCA CCTTCTATGA GAACATTATT AGATTCCATT 780 GCTCCAGCAG GAGTTGATGT AGTTACAGAA TATGTGAAGG CTTGTAATGG GATTGGAGGA 840 GCCATGCATA AAGCTATCCT AATGGCTCAA GCAATGACTG GGGTTGCTTT AGGAGGACAA 900
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