Tag | Content |
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EnhancerAtlas ID | HS129-01072 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:46504630-46505710 |
Target genes | Number: 14 | Name | Ensembl ID |
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SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr1:46504933-46504947 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH01I046039 | chr1 | 46504935 | 46505626 |
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Enhancer Sequence | TAGGTTTGGT GGTAGGAAGG TGAGGAAATT CATAGCCAAT CATACTTTTT CTGACAAGTA 60 AACAAGTTTG CTTTTTTGAG ACAGAGTTTC GCTCTGTTGC CCAGGCTGGA GTGCAGTGGC 120 ACGGCCTCAG CTCACTGCAA CCCCTGCATC CCAGGTTCAA GCAATTCTCA TGCCTCAGCC 180 TCCCGAGTAG CTGGGATTAC AGGTGCATGC TACCACGCCC AGCTAATTTT TGTACTTTTA 240 GTAGAGACGG GGTTTCACCA CGTTGGCCAG GCTGTTCTCG AACTCCTGAC CTCAGGTGAT 300 CCACCCGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCA TGAGCCACCA CGCCCAGCCC 360 CAAGTAAACA AGTTTGAAGT GTCGGTGAGA TACCCAGGAG CCCAGTGGAA ACATCCAGCC 420 AGCGGGTAGA GTTCAGAAGA AAGAACTGGG AAGGAGCTAG GAATTTGAGC ATCCTAAACA 480 CAGAAGTGCG AACAACTCTG GGATTAGGAG AAATCCATAG TTCCTGGCAG TGGTCTTGGG 540 ATGCTGTGTA GCTAAAGTGT AGTGGGGAGA AAAGACATAG GCAAGGTCAC TTAGAACAAC 600 AGGCTGTTCC CTGCCCAATC TGACTTATTT ATAATTGAGT ACACATGGGT GGGGCCTGAG 660 ACATGGATGA GCGCTGCAAT ATCCTATGCA ACAAGAGGTT ATCGCATGTT GGCTCATTAC 720 GTTCCCAGAA TACAGGAAGC TCAACAGTGT GCCTTGGCAG GAGATGACAA GGGCCTGGGG 780 CAATAAGAGG ATAGATTATA AAGCTGGGCC CATTTCCCCC TCCCCCAGAG TAGAATGTGG 840 AAACACTTCA TTCTGGGCAG AAATATGAGA ACCAATAAAC AGCTTATTAG GAGTGGGCAG 900 TGAGGTGTGG AGGAAATGGC ATTCAGTTTT AATTTTCTCA GAGTCAGTAT CTAAGACTTC 960 TGTGTCTGTG TTCGGTGGAC AGGACTCTGG CATCATGCCT AGTTGGAGTC AATGTCCTCC 1020 CCTAGGAAGA AAAGAGCCTC TGGCTGCCCC AGTACTAGTC TTTTGGTGCT TACTGGAGAG 1080
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