Tag | Content |
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EnhancerAtlas ID | HS121-23291 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr2:242176180-242178060 |
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) |
Myog | MA0500.1 | chr2:242176212-242176223 | GACAGCTGCTG | + | 6.14 | Sox3 | MA0514.1 | chr2:242177318-242177328 | AAAACAAAGG | - | 6.02 | Tcf12 | MA0521.1 | chr2:242176212-242176223 | GACAGCTGCTG | + | 6.02 | ZNF740 | MA0753.2 | chr2:242176392-242176405 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr2:242176393-242176406 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr2:242176394-242176407 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr2:242176395-242176408 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr2:242176396-242176409 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr2:242176399-242176412 | GGGGGGGGGGCGG | - | 6.64 |
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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 | TGAACTAGAG AGAAAGGGGA AAAGGGACAG CTGACAGCTG CTGGAAGAGA CCCCACACCT 60 TGTTCAGAAT GCATATGTCT GTGAGGCACC TGCTGGGTGC TGGGTGGTAA AAGGGAGGGA 120 AAACCACTCC TGTCCTTCAG GAGGTCTTGG TCTGGTCAGG GAGAGCAGAT AGGACGTCCC 180 CACAGCAGCC TCAAAGAGGG CTCCCAGACC TTGGGGGGGG GGGGGGGGGC GGCAATGAAG 240 GCTTTGCCGG GAGGCCGTGA GCTCTGTGTC TCCCTTCTTC ACCTTGAAGA TGAAGCTAAC 300 AGCAACTAAC TACAGCAGAG GCTTCAGTGA GATCAGATGA GTTAGTTCAT GGGAGGAACA 360 CAGGGCAGAC CCACTGCACA AGTGAGGCTT GACTGTGAGG CAGGGCTCAT CAGGGAAGGC 420 GGCCAGCACG CAGCCCCACC CAGGAGAGGC AGTGGGAAGG GGGGTGAGAG GTCTAGGGGA 480 GACAGAAAGG GCAAGGCCAA GGTAAACCTG TGCCAGCTCC TTATGCCAGA AAGCGAGAGC 540 CCCAGAAGTG AAGAGGCGTG TGAACAGGAC ACAGAAGACA GCTGGAGGGG CTCCTACAGG 600 CCACACTGGG ACACCGCGTG TGTACCAAAA TAGACACCAC AACAATAAGT GTCACAAAAC 660 AGACACAACA ATAATTATCA CTAAGACAGA ACCCAGGAGG TGTGTGATGT AAATAAATGA 720 GCAGGAGACC AGACAGACGC CTGCCTGAAA TCAAGGGTGA TCCTAGGATG GGGAAGTAGG 780 TGTTTCTGAA GGAGAAAAAC TGGCAAATTT GAATACCGAC AACATATTAG ATACTACTGT 840 TATATAATGT TAAATCCGAT TCCGATAAAT GTGCTAGAAT TATGTAAGAG AATGTCCTTG 900 TTCTAAGAAA ATACCCACCA TGAATAAAGG GACATGTCTA AAAATGACAT TCAGAAAAAA 960 AACGTGTGTA AAAGGGGAGA AGTTGAGAAA AGAAACTGGT GCCACAGGAT GTGTCTTTAT 1020 ACTATTCTGT GAAATTCTAT CAAAATCAAA GTTTTAAATA ACCACTGAAG TGTAAAACAT 1080 AGACAGAGTG CAGTATGAGT TTATTAGTTT CCTACTCAAA ACACCCTGTA TTCTCAGGAA 1140 AACAAAGGGG CTTGAATGGC TGTGTGTGAC ATGCTTCCTG GATGCCCAGA GAGATGACAC 1200 TATGTGCACT CAGCAGGCTG CAGGGCCACC TGCCGCCCAA ACAGCTCAAC CAAGACTGAT 1260 AACACAGAGT GGAGGGCGGG CATCTGATAA CACAGAGTGG AGGGCATACC TTTTGTTTCA 1320 CAAATGCAGA GCAAGTGAGA GAGAGGCAAC CGACCCGCAT CCCACAGGTC GCCTCCCCAC 1380 CACCAGGTGC ATGAGCAGAG CTGGGGGCAA GCATGGTACG GGGAACTGAA TGCTCTCCTA 1440 GAACTGCCGG CCACTTGGAT GGTGCCCTCT GGCCAGCCAG AGGCTGCAGC TGCCTGCCTC 1500 ACAGGGGACA CCCCACAGTG ATGGGAGATG TGGAGGAGGA AGCTCTACGA CGGGGCTCAT 1560 GCGATCCAAA CGATGTCATG AGAATCACTG GGACTGAACT CGGGACACCC GAGGATGAGG 1620 CTGCACGCTC CTCATCGCCT TGGGACTGGC TACCTTGTGT GTCTCTAGGA CCTATGAAGG 1680 TCACCTGGTC ACTCTGTCAG TAACTGACGT GGTCCATCTT TTAAAGGCCA GGGAGTGACC 1740 CTGAACCTCT GGAAGCCCCC AGAATACATA GATGGTTTTC CAGCAGAGAC AGGAAAGAGC 1800 CTCACCAGTA TGTGCGACAG CCCCGCCTCT CACATGGGAG GCGCCACTAT TAACAAGCAG 1860 AGCAGGGCTA ATGGGGGACC 1880
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