Tag | Content |
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EnhancerAtlas ID | HS187-08994 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr16:2976710-2977310 |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I002926 | chr16 | 2976509 | 2978253 |
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Enhancer Sequence | TTAATGGCCT ATGAAAATGC AAATCCGGAA TGTCAATTGG CCATAAAGCC ATGTTGACTA 60 CAATCAATTA CAGGAGGTAA CATATCCTGA ATCATCAAAA TTGGGGGGAA AAGTGGGGCC 120 ATCAGAGTCT AAACCACAAT GGCCAACTCC TCCTCCCGTG GTTCAGATAC CTGTAACATT 180 ACAACCTCAA ATGCAGGTTA GACAAGTACA AACCCCAAGA GAATATCAAA TAGAAAAGGA 240 TAGTCTCTAT CTCGGCAATG CCAATCCAGA TACAGTATCC ACAATATCAG CCAGTAGAAA 300 ATAAAACCCA ACCGCCATTA GCTTATCAAT ACTGGCTGCC AGCCGAGCTT CAGTATTGGC 360 TGCCTCCAGA GGTCCAATAC AGACCTCAAG TGGTGTGTGC CATGCCAAAT TGCACGGCAT 420 CGTACAAGCA ACCCATGGCG GTGGTGTTTA ATACGTCAGC ACCACAGGGC GCGGCGCTGT 480 GTCCTCAGCC GCCCACTATG AGACTTAATC CAACAGCACC ACCTAGTGGA CAAGGTAGCA 540 CACTGCACGC GATCATTGAT GAAGCTAGAA AACAGGGAGA TCTTGAGGCG TGGCAGTTCC 600
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