Tag | Content |
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EnhancerAtlas ID | HS128-00179 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr1:15831570-15832480 |
Target genes | Number: 11 | Name | Ensembl ID |
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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) |
RUNX3 | MA0684.1 | chr1:15831889-15831899 | TTTGCGGTTT | - | 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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Enhancer Sequence | AAGAAATGTG ATTCCTGGGC CCCACCCAGA CCTCCTAATC AGCAGTATGG TCCTCCAGGC 60 CCCTCTGACT GAGGCAGCTC AACGCTGAGA GTGGCTGCTT TAAATCAGTT CAGCTCAGAC 120 CTCAAGGGCA TGGAAATCAC CTGGAAACCT TGTTGCTGGG CGGACTTGGA ATGAAGAGGT 180 CCAGGGTAGG GCCTGGGAGT CCACATTCTT CATGAGCTCT AGGGACCATA TTATGAGAGA 240 AAGGACCAAA GGGAAAGCCC TGCCCAGCCA CAGGCTGGAG TTTTACTGGC TGAAGATGCT 300 GGCCTCGTCA GGCCAGACCT TTGCGGTTTG TCAAGAGAAA CTAGAAATCC TGATTTTTAT 360 GTGAAATTTG CCAGTTTTCA AAACACCGTG CAGACCACAG GGGGACTCCA GGCCCCAGCT 420 TATAACTGTG ATCTGTCCAA CTCCTCAACT TAAAAGATGA GGAAACTGAG GCCCAGTAAG 480 GGGTAAGGGC TTAATCACAG TGACAAATAC GTAAGGGGCC AAGCCCCCAG TGGGCCTGGT 540 GTCCTGAGTC CCACCAGCAG CAAGGGGCCT GGGGCAGTGC CTCACAGGAC AGAGACAGGA 600 GCTGAGACAA CATGTGTGCT GTACCCGCCT CTGAACAAAC TCTGGGTGCA GGAGCTTCGT 660 GAGCAGACCT GGTCTCTGCC CTCCCTCTCC CAGAGGGCTT CTCCCAGGAA CACCGACCTG 720 CCCAGGACGG TGCAGCCAAC TCCTCAGAGG ACCACATGGC TCCCAAGAAA ACAACAGGAG 780 GTGGGCAGGG CCCCACAGCC CTTTTCCACA AAGCCAAGGG TGTTTTGGAC ACAAGAAGGG 840 ACATGGCCCC TGCACAGCCT CTTGGCACGG CCAGTACCCA ATGCCTGCCC AGGGAACAGT 900 GGGAGGCTTC 910
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