Tag | Content |
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EnhancerAtlas ID | HS184-02802 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:229980120-229981060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | + | 8.23 | Ar | MA0007.3 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | - | 8.58 | Foxq1 | MA0040.1 | chr1:229980815-229980826 | TATTGTTTATT | + | 6.62 | NR3C1 | MA0113.3 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | - | 7.22 | NR3C1 | MA0113.3 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | + | 8.14 | NR3C2 | MA0727.1 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | - | 7.35 | NR3C2 | MA0727.1 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | + | 7.67 |
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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 |
GH01I229843 | chr1 | 229979382 | 229980770 |
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Enhancer Sequence | TAATCTGCTT TTCTTTCCAT CGACTTTTAG TGCTTTTAGT GTCTTTGGTG TGGAGGGAAG 60 GCATGGCAGG AGGCAAATCT CCAAATTTTT CTTGGCCAAC CCAGCTCTCT CCCCTCTTGC 120 CTGCAATTCT CAGAGAGAAG GTACTGAGAA TGCAACACCC TGAGATAAGC AGGAACCATC 180 TGAAACAGGC TGGGATTTAT CCATCCAGGA CATCTTCCTA GAACAGGATA TCCTGCAAAG 240 CTTGGGCTCA GCAAACCATG TTGCCCCTGG GGTATAAAAA CCAAAACACA GCCCTTTCAG 300 GGTCTCTCGG CTGGGATGCG AAGTGAGGCA CGTGTAGACA AGACTCCATC TGCCCTGGGC 360 AGCTTTCCTG AACCCGAGGG ACTGGTTTGC CATGGATCCT CGGCTTCTGT TTATCTTTGC 420 TGCTCACCTG TGAGTTGTAA ATCTGCTTTG CCTGACTTGT GTGACAGTTC CATCTCACCA 480 GACTCACTGG GACAGCCGGG CTAGTGCAAA ACCTCCTGCT AGACCTGGAA GCCTGCCATA 540 TCTAGGAACC TTAGCAGAAA ATGCAAGGAC TTTTGAGTGT TCCTCTAGGA TTAGCAACAG 600 GTACACAGTG TTCCCCTCAC AGGGATTGAT ACTGATGTAT GTTATTCTGC TTCACAGGCA 660 CTGTTTAGAG TTTTGCAGAC TGAGTGTTCA TTTCTTATTG TTTATTGTTC TTGAGATTCC 720 TTGGTGTTGC TGAATCTAAG GATTGGTGTC TTTCATCAAT TCTAGAAATT TGTTGGTCAT 780 TATTTCTACA AAGTGTGGCT TTTCTCTGCT GTTTCTATTA TGTTCTTCTG ATGTTCTAAA 840 AACATATATT TTGGGTCTTC TTTCTTGGTG ATTTATTTCC GTTGATACCT CTTTTTCATG 900 TTCTCTGTTT GTCTCATTTT GTGTGCTATT TCTTAATATT 940
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