Tag | Content |
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EnhancerAtlas ID | HS129-24766 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr3:14240050-14242120 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr3:14241051-14241069 | TACATGCCCCTGCAAGTT | + | 6.14 |
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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 |
GH03I014199 | chr3 | 14241114 | 14242938 |
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Enhancer Sequence | CCAGAGTTTT ATCAAAATGC TTTCTGGGCC AGACATGGTG GCTCATGCCT GTAATCCCAG 60 CACTTTGGGA GGCCAAGGTG GGTGGATCAC CTGAGGTCAG GCGTTTGAGA CCAGCCTGGC 120 CAACATGGTG AAACCCTTTC TCTACTGAAA ATATAAAAAT TAGCCAGGCG TGGTGGCGCA 180 TACTTGTAAT CCCAGCTACT CAGGAGGCTG AGGCAGTAGA CGCTTGAACC CAGGAGGCAG 240 AGGTTGCAGT GAGCCAAGAT CACACCATTG CACTTCAACC TGGTCAACAG AGCGAGACTC 300 CGTGTCAAAA AAAAAAAAAA AAAAGTTTTC TGCCCTCAAG TCTTCTGGGG AGGCAGATGT 360 TTAAACCAAC AATTGCAGGC AGTAAGATTA GTGCTGATAG AATCATGCAC ATGCAGGATG 420 CCATAGGAGC ATGGGGAAGA GCACCCAAAT ATGGGAGAAA GGGGCAGAGG GACATTGTAA 480 ACATCAACCC TGCAGTAGAA GACAGAGCAA AGCATGATTT CTCTTTTCTC TGGCCTGATT 540 TAATTCTAAG GTCAGACGTT CAGCTTGATC ATAACCTGTT TATAATTATG ACTCAGACCA 600 TTTTTCCACT CTTGGATCAT TGGCCATTAA TGATGAGGGG TCTCAAACAA CATGTCTCAG 660 TGACACAGTA AAGCAGAAAT TGGCTGAAAG CAAAGCTGTT TTTATTTCTA GCTTCAGTCA 720 GCACATAATG CTTAAAACCT AAAGAGGAAA GTAAAAGCGT GTTACAATCT CTCAAACTTT 780 ATCAAGACAG GGCTTAGAAC CTGACATCCT CCGCTATGGT CATTCCATTT TGAAATGTAG 840 AAAATCCAAC TTGTGGATGG TTTGTCTGTA AATGAGCTGA ATGTGTGTGC GTGTTCATTA 900 TCAAGCACGA TATGCTCACA AATGCACAGT ACTTTAAGCC TTGTGCAAGA AAGATGCTTT 960 CAGTAAACAT ATTTAAAAGG TTTTATTTTC CTTACTAATG GTACATGCCC CTGCAAGTTC 1020 ATGGAGAAGA GAAAAACAAG TGTGGGTGAG CTGATGGAGG CTTCATCTTA GGTGAGGAGG 1080 CAGGAGAGAC ACCCTCCCTT CACTTGTGCC ATCCCCACGC TTTGTCCTTA AGCTGTAGTG 1140 GTCCCAGGAG ATAACCTGTT TACAGCAGCC CATTCAGTAT TGAAAAATGA ACTCCCTCCT 1200 GCAGAATGTT AGAAGAAACA ACCTCAAAGA CCTCAGGCCG CCTGTGGTCA TTAGTATGTG 1260 GCAGCAAGAT TGAACCTGCC TGCCTCCTAC CTGTGTGAGC CTGTGGTGTG GGTGTGGTAC 1320 CAAGGCCCTG GCTCTGGGCA GTCTGTTGGC TCCTGGTGTT CACTAAGGCG TGGGGTGACA 1380 GGCCATCTGG CCTCGCTCTG CCAGTCTGCA GTTCTCCCCA GCACTGCATT CATTTTTAGT 1440 GGTTTCTGAT AGTCACACTG AATTCCTGGA CACTTTCTTC TCTTCATTCT TAGTTATCTT 1500 TCTCCTTTTT CTCCTGGAAC TGATAGTTTA CACTAAAACT TTTGGCTGTG AGGACTTGAT 1560 TATACACATT TCTAAAACCC ATGAACCTTA ATATCTGACA CTGTTACTCT CATATGCACA 1620 CACAACTAAA ACATACCAAC CTACTTCATT TCCTAGCTGC TAAGATACAA GGGGAGGGAC 1680 AATAAAAGGT TAACTGCAGA ATAGCCACCT ATGTGTCAGG AAATGGAGGG AGGGGAGGCA 1740 ATGTGTGAGT CCTTTTGGAG CTGGGACTCA ATCCACAACA GAGACAGCTC AAGCAGGGCC 1800 CTGCCATGGT CCACACTGAG GTTTCCTCTG CAGTGGTGCT GTCCACTGAG GGGTTATGGT 1860 GTGAGGGCCC CTGGGAGCCA CGCCTTGGAC TTCTGAGTCT GCAGAGCACT CGGCTCCAGC 1920 CAGCTGGATG GCAGGTGGTC AGTGGAGCTG GTGACTGGTG GTTTCTGCAA TGAGGTGTCA 1980 GATTAGCCTA AGGGAAGCCT CTTCAGCAAG TATCATGCCT GGATCCCGGT CTTGGTTGTT 2040 TTATGAGAGG CCGATATGAA TTGCCATTGC 2070
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