Tag | Content |
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EnhancerAtlas ID | HS129-03339 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:212360750-212362350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF3 | MA0522.2 | chr1:212361237-212361247 | AACACCTGCT | + | 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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| Number: 3 | ID | Chromosome | Start | End |
GH01I212186 | chr1 | 212359743 | 212360831 | GH01I212187 | chr1 | 212360943 | 212361742 | GH01I212188 | chr1 | 212362101 | 212362250 |
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Enhancer Sequence | AACCTCCGCC TCCCGGGTTC AAGTGATTCT CCTGCTTCAA CCTCCCAGGT AGCTGGGATT 60 ACAGGTGGCC TGCCACCATG CCCAGCTAAT TTTTGTATTT TTAGTAGAGA TGGGGAGACG 120 GGGTTTCACC GTGTTGGCCA GGCTGGTCTC AAACTCCTGA CCTCAGATGA TCTACCCGCC 180 TCAGCCTCCC AAAGTGCTAA GATTACAGGC GTGAGCCACT GCTCCCGGCC CTCAAAAGGT 240 GATCTTTAGT ATTTTTAGTA GAGACAGGGT TTAACCGTGT TAGCCAGGAT GGTCTCGATC 300 TCCTGACCTT GTGATCTGCC CATCTCGGCC TTCCAAAGTG TTGGAATTAC AGGTGTGAGC 360 CACTGCACCC AGCCGCATTG GCCAATATTT GACAGTGCCC TGTGAAAGGA TTGGCAGGAG 420 AAGAAAATAA ATAGGAAACA GTTTTCCAGC CACAAGAAAT TCAACTCAAT TCAATCAAGG 480 CTGACTAAAC ACCTGCTGCA TCTAAGTCCT TGAGCCAGGG TGGGCTTCTG TCCCTAGCAG 540 AGGCTCTTCA GCCTGGAGGC GCACCGCTGG GCTGGGGCAG GACCAGTTAA AAGTGAGGAA 600 ACCATACATG TACGTCAGAG ATATGTTTTC TCTCTTTTCC CTTTGGGAAG ATGTTCTTGG 660 GAGTTCTTTG CCAGGAAGTT GGTCACTTCC TGCCCAAATG ATGAGGTTTC CAAAAGGTAT 720 AAATAGATTC ACTTGCCACA TGGAATTGGC TGAAGATGCC TCCACATGCC AGAAGGAAGC 780 CTTGGGAGGG TTCTTTCCAG TATCAGGGAG CTCAGAGACA GGAGGCAGCA GCTGCCAGAG 840 AAGCAGCACC AGCACCAGCC GGGCCCAGTG GGCTTCAGGG CTGAGGGCAA AAGGGCCTGG 900 AAAAGTAACA AGTCTGTTGC GGAAAGTGCC GGGACTAACG TGCTGTGAGT ACGGTGAAGC 960 ATATGAGAGA AAAGAGCATA GTAAATGATG AATAAGTATA AGAAATGCGG CCGGGCGCAG 1020 TGACTCACAC CTATAGGCCC AGCACTTTGG GAGGCCGAGT CGGGCAGATC ATCTGAGGTC 1080 AGGAGTTCGA GACCAGCCTG GCCAACATGG TGGAACTCTG TCTCTACGAA AAATGCAAAA 1140 ATTAGCTGGG CATGGTGGCG CACACCTATA ATCCCAGCTA CTCTGGAGGC TGAGGATGGA 1200 GAATTGCTTG AACATGGGAG GTGGAGGTTC CAGTGAGCTG AGATCATGCC ACTGCACGCC 1260 AGCTGAGGCA ACAGAGTGAG ACTTCGTCTC AAAAAAAAAA AAAGTAAGAA ATGCGTTTGT 1320 AAGGATCTGC AGAAGGAAAA AAGAAGACTA CTAGAAATGT CAGTACCTGC TCAGTGAGTC 1380 ATGCAGGGTG AACCACATAC AGGAAGGGGT CAGAGGGTGC AAGAAGGGGA AGAACATGAT 1440 AACTTATAGG GCCAAAGGCT GTGAGACTCA CCTGGTTGTG CTAAAGAATT CTCCATGTAG 1500 GCATTGGTGT TACATTCAAA TTTGTGTTGC ACATATATTG TTTTTGTGTA ACTTTAAGTG 1560 CGTACTAAGT TCTATTGGTA CTTTATCCAT GGGAGTAATT 1600
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