Tag | Content |
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EnhancerAtlas ID | HS003-16869 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr16:2976740-2978120 |
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) |
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 | TGTCAATTGG CCATAAAGCC ATGTTGACTA CAATCAATTA CAGGAGGTAA CATATCCTGA 60 ATCATCAAAA TTGGGGGGAA AAGTGGGGCC ATCAGAGTCT AAACCACAAT GGCCAACTCC 120 TCCTCCCGTG GTTCAGATAC CTGTAACATT ACAACCTCAA ATGCAGGTTA GACAAGTACA 180 AACCCCAAGA GAATATCAAA TAGAAAAGGA TAGTCTCTAT CTCGGCAATG CCAATCCAGA 240 TACAGTATCC ACAATATCAG CCAGTAGAAA ATAAAACCCA ACCGCCATTA GCTTATCAAT 300 ACTGGCTGCC AGCCGAGCTT CAGTATTGGC TGCCTCCAGA GGTCCAATAC AGACCTCAAG 360 TGGTGTGTGC CATGCCAAAT TGCACGGCAT CGTACAAGCA ACCCATGGCG GTGGTGTTTA 420 ATACGTCAGC ACCACAGGGC GCGGCGCTGT GTCCTCAGCC GCCCACTATG AGACTTAATC 480 CAACAGCACC ACCTAGTGGA CAAGGTAGCA CACTGCACGC GATCATTGAT GAAGCTAGAA 540 AACAGGGAGA TCTTGAGGCG TGGCAGTTCC TGGTAATTTT ACAATCGGTA CCGGCCGGGG 600 AAGGGGCTCC AGCAGGAGCA CCTGCGGTGG CTAATGCTAG ATATGAACGC TTCACCATGA 660 AAATGTTAAA AGACATGAAG GAAGGAGTTA AACAATATGG ACCCAACTCA CCTTCTATGA 720 GAACATTATT AGATTCCATT GCTCCAGCAG GAGTTGATGT AGTTACAGAA TATGTGAAGG 780 CTTGTAATGG GATTGGAGGA GCCATGCATA AAGCTATCCT AATGGCTCAA GCAATGACTG 840 GGGTTGCTTT AGGAGGACAA GTTAGAACAT TTGGGGGGAA ATGTTATAAT TGTGGCCAAA 900 TTGGTCGTCT AAAAAAGAAT TCCCCGGCTG GCTCAGTCAG TAGATCATGA GACTCTTAAT 960 CTCAGGGTCG TGGGTTCACG CCCCACACTG GGCGCCAGGT GAAGGAGGCC TGCCGCTCCA 1020 CACCTATGGA TATTTCTCGT CAGGTGGAGA TGAGACTGAT AAAAGAAATA AGACACAGAG 1080 ACAAAGTATA TAGAAAACAG TGGGCCCAGG AGATGGGCAC TCTATGTGCG AGGACCCGCA 1140 CTGGCGCTGG TCTCTGAGTT CCCTCAGTAT TTATTGATGA CTATTTTTAC TATCTTGGCA 1200 AGGGGAGTGT GGCAGGGCAA CAGGGTGATG GTGGGGAGAA GGTCAGCAGG GAAACATGTG 1260 AGCAAAGGAA TCTGTATCAT GAAGAAGTTC AAGGAAAGGT ACTGTGTCTG GATGTGCATG 1320 TAGGCCAGAT TTGTGTTTCA CTTCACACAA ACATCTCAGT GTAGCAAAGA GTAACAGAGC 1380
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