Tag | Content |
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EnhancerAtlas ID | HS129-02632 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:180540700-180542160 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:180540835-180540856 | AAGAGGAAAAGGAAACTAAAA | - | 6.12 | YY1 | MA0095.2 | chr1:180541130-180541142 | CAAGATGGCAGC | + | 6.32 |
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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 |
GH01I180570 | chr1 | 180539881 | 180541895 |
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Enhancer Sequence | TGCCCCCAGC CTCTGTCATC ATCCTTTGCC CTCTCACTCT ACGAGGTCCT TGGCTGACCT 60 GATCCTTTAC TGTGGTTTCA ACTTCCTCCC ATAGGTTGGT GACTCCCTGT GTGATTTAGG 120 ATTACATGTG GCTGCAAGAG GAAAAGGAAA CTAAAATACT GGGAGCTTAA AAGCTTAAGC 180 AAAAGCTAAG TTTTAAAATG TATTTTTCTT TCTCACATAA CGTCTGAGTA AACAGTCCAG 240 AAGCTCCGTG AGGTCTGAGA TCCTCTCTCT GGGCCTCCCT TTACAGCCTC AGAGGCTGAG 300 TGCCGAGCAG CTCTAGCAAG CGCGATTCCC ATAGACAGCC TGAGTGGTTC CTTCTGGAGT 360 AGAGCAATGT GATGGCCCTG CCCAGGACCC TTCTCTCTTG TCTTCTTTAA GTGGTCTCAT 420 CTGTGTTGTC CAAGATGGCA GCATTTATCT TCCAGGAAGG AAAATGGCAG AAGGGACAGA 480 GGCAGATGAA GGGGCGCAGG GTACACGTGG GCTGAATCTT AAGTAAGGTT TTCAGAACTT 540 CTCATTGTCT TAGTCATATG ACCATACTCA GTCTTAATCA TACATGTCTT AGTCATAGGA 600 CCATACTCAG TTGCAAGTGA AACGGGGAAA TGTAGTTTTT ATTCCAGGTG GCCATGCACC 660 CTTCCCCCCA GAGAAAAGCG AAGGGAGGGA AGGAATCCTA TTACCATGAA ATAAGAATAA 720 ACAAGTATTA GGGGACAACT GGCAACCTTG GTTGCTATTT CCAATCTATA CTTCTAGTCC 780 ACACCCATAT AGTCAATTGT CTCCTGGACA CCTCTACACA GATGACTCAC AGACAGCTAA 840 ACAAAACCAG CCCTAAATGG AAAGTGTTGT GCTTCCCCAC CTACTCCCGT CCCAAACCTG 900 CTCCTCCTCC TGCGATCACC ACCTCAGTGA ATGGTAATGT CATTCATCTA CTCGGATGAG 960 AATCATCTTA GACTCTTGCA TCTCCTTCAC TGCCTGTCCT CTCTCCCTGC CCTGAGAGTG 1020 CCACCCCTGC AAATCTCCTC CTCCCCATCC CCATGACTTT AGCTGAGACT CATTTTTTTG 1080 CTGGTCTGGA TTACTATAGG GGCCTTAAAC CGGACCTCCT ACCTCCAAGT TGTCCCCACT 1140 ACAGTCTTTT CCCCACCTTG TGCCCAGAGT ACTCTTGGTG AAGAGAAACC TAATTTTCAC 1200 CTACCCCTCC TTCGAACTCC TGGGTTTCTC TGTACCTTTG GTGGTAAAGG GGTTTCCTCG 1260 TACCTTTGGT GGTAAAGTTC ACTCTGTTTG AGCATAGCAC CCGAGGCTCG TCAGGATCTG 1320 GCCTCTGCCT GCCTCTCCTG CTCCATGTGC TACCTCTCCC TACCACACAA CCTTTGATCC 1380 AGTCCAATGG TGCTGAACTA TGGGTAACAG TTCCCTAAAC AGCCAGCTGA TGCATGCCAC 1440 TCTGCCCCTG CACAGCTGCC 1460
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