Tag | Content |
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EnhancerAtlas ID | HS129-11067 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr14:23367460-23369070 |
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) |
EWSR1-FLI1 | MA0149.1 | chr14:23367966-23367984 | GGAAGGCAGGGAGGCAAG | + | 6.41 |
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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: 2 | ID | Chromosome | Start | End |
GH14I022896 | chr14 | 23366207 | 23368602 | GH14I022899 | chr14 | 23368963 | 23369927 |
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Enhancer Sequence | TTTAAAGAAC AGGGAGGAAA TGCTGCCACC TTAGTGAATA CAGAAGCATA GACTGGAAGT 60 CAAAAATCAG GTGAGAATCT TTTCTAGAAC TGAAGACTGG TAGGGAAATT CTAACTATGC 120 TGGCAAAGGA TCTAGATCAC AATGTCACCC CTACGCCACC AGCCACCATG TGCAGGTAGA 180 TGTTGAGGGA AGTTTCTTTT ACCTTAAGCT GGGCCCAGAG TCTGTTCACA GCCCGCTTCT 240 CTCCACTCTA ACCACCTCGT ATGGAGGGAT GAGTAACAAG AAGGCACTGA GTCACACACG 300 GACAGCAACT GTCACTCACT AGATACCATC ACCTTATATG GAGTAAGACT GGAAATTGTC 360 TTAGATACGT CCTTACTTCC AACATTGTCT CTCTCCCAGC AAGAGGCTAT GTGAGGAACT 420 AAGAACAAGA AAGAACTGAG GTGGAAGGAT CCGAGTGTAG GAAGGCCAAG GTAGCTAGGG 480 ATGGAAACAT AAGGAAACCA AGCAGAGGAA GGCAGGGAGG CAAGGCCTGT GGATATTTAT 540 AATAGTCTGA AGGAGCCAAG CCAGCCATGA GAAGACCCAG TTCATGGCCT CAGGATGACT 600 AACAAAAACG GTACCCACTG CACTTCTCAA GATACATTAG AAGCCAAATC AATAACTGTA 660 GGGGTGCTGG GTCATAGCCA GCAGCTTCTA CCTAAAAATA GTGCATCCTC CTTCCCTTTT 720 CCCCCGGTCC AGAAAGCAAA CTAGGATAAG ATGGGGGAAG GGATGGGGGT GGTAACCAGG 780 AGAACAGCAA CATCATGTGA GATCTAGGCC TGGAAGAATC AGAAATGCTG TGGTTTGAAT 840 GTGTCCCCCA AAAGTTCACA TTGGAAATTT GACTCCCAAT GCAACAGTGT TGAAGATGGG 900 GCTTAATACG AGGTGACTGA GTCACAAGGA CAGAGCCCTC ATGAGTGGAT TAATGTCACT 960 ATCACACAGC AGGTTATCAT GAGAGAGGGC TGTTATAAAG CAAGTTTGGC CCATGGTCCC 1020 TTTGTCTCAT GTACTCATTT CTACCTTGTG CCCTTCTGAC ATGGGATGAC CCCCACCTGA 1080 TGCAGGCACC ATGCTCTTGA AATTCCCAGC CTCCAGAACT GTGAGAAATA CACTTTTCTG 1140 TTTTTTTGAG ATGGAGGCTC GCTCTGTTGC CCAGGCTGGA GTGCAGTGGT GCATCCTCGG 1200 CTCACTGCAA CCTCCGCCTC CCAGGCTCAA GCGATTCTCC TGTCTCAGCC TCCTGAGTAG 1260 CTGGGATTAC AGGCACCCAC CACCATGCCC AGCTACTTTT TGTATTTCTA GTAGAGACAG 1320 AGTTTCACCA TGTTGGCCAG GCTGGTCTTG AACTGACCTC GTGATCCACC CACCTCGGCC 1380 TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CAGTGCACCC AGCCTACACC TCTTTTCTTT 1440 ACAAATTAGT CTGTGCTATT GTTACAGAAG CAGCAAACAG ACTTAGGAGC TAGAGTCCCA 1500 CTGGCCTTTT ATGACTCAAG CAGGCTTCAA GTATTTAAAT GATTTTGTGT TAAAAGCAAC 1560 CCCAGAGGCT AACATCACTG GCTTAGAAGT CTGAGAGCTG ACAAATTAAA 1610
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