Tag | Content |
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EnhancerAtlas ID | HS062-06038 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr16:2976730-2977700 |
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 | AAATCCGGAA TGTCAATTGG CCATAAAGCC ATGTTGACTA CAATCAATTA CAGGAGGTAA 60 CATATCCTGA ATCATCAAAA TTGGGGGGAA AAGTGGGGCC ATCAGAGTCT AAACCACAAT 120 GGCCAACTCC TCCTCCCGTG GTTCAGATAC CTGTAACATT ACAACCTCAA ATGCAGGTTA 180 GACAAGTACA AACCCCAAGA GAATATCAAA TAGAAAAGGA TAGTCTCTAT CTCGGCAATG 240 CCAATCCAGA TACAGTATCC ACAATATCAG CCAGTAGAAA ATAAAACCCA ACCGCCATTA 300 GCTTATCAAT ACTGGCTGCC AGCCGAGCTT CAGTATTGGC TGCCTCCAGA GGTCCAATAC 360 AGACCTCAAG TGGTGTGTGC CATGCCAAAT TGCACGGCAT CGTACAAGCA ACCCATGGCG 420 GTGGTGTTTA ATACGTCAGC ACCACAGGGC GCGGCGCTGT GTCCTCAGCC GCCCACTATG 480 AGACTTAATC CAACAGCACC ACCTAGTGGA CAAGGTAGCA CACTGCACGC GATCATTGAT 540 GAAGCTAGAA AACAGGGAGA TCTTGAGGCG TGGCAGTTCC TGGTAATTTT ACAATCGGTA 600 CCGGCCGGGG AAGGGGCTCC AGCAGGAGCA CCTGCGGTGG CTAATGCTAG ATATGAACGC 660 TTCACCATGA AAATGTTAAA AGACATGAAG GAAGGAGTTA AACAATATGG ACCCAACTCA 720 CCTTCTATGA GAACATTATT AGATTCCATT GCTCCAGCAG GAGTTGATGT AGTTACAGAA 780 TATGTGAAGG CTTGTAATGG GATTGGAGGA GCCATGCATA AAGCTATCCT AATGGCTCAA 840 GCAATGACTG GGGTTGCTTT AGGAGGACAA GTTAGAACAT TTGGGGGGAA ATGTTATAAT 900 TGTGGCCAAA TTGGTCGTCT AAAAAAGAAT TCCCCGGCTG GCTCAGTCAG TAGATCATGA 960 GACTCTTAAT 970
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