Tag | Content |
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EnhancerAtlas ID | HS175-23275 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr5:21119820-21121240 |
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) |
MEF2A | MA0052.3 | chr5:21120895-21120907 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr5:21120895-21120907 | TCTATTTTTAGT | - | 6.32 | ZNF263 | MA0528.1 | chr5:21119968-21119989 | GGAGGATGAGTTGAAGAGGGA | + | 6.11 |
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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 | CACAATAGCC AATAAGGTGT TAGACCAAGG AAAGCAACTT TGTGTTGAAG AGGAGCAAGC 60 CAAGAAATGG AAGACTAGTG TCCTGAAGAG TCATCTTAAA AGGCCTAAAT CTCATGCTTC 120 TTTTTATATT GGGAAGGGAG AACAATGAGG AGGATGAGTT GAAGAGGGAA CAGGTGACCA 180 GATATTTGTG CATCAGCAGG TGTCTGAGGG GGGTCGCATA ATTTCTTTGG CCTTGGTCAG 240 GTCACGATGC TTCTATAAAT CTGTAACATT ATATTGTTAC TTTTGTGTAC CATCTCCTTA 300 TTTCCTCAGC AGTTAGTTTA GGGAAGGGAC TATTATCATT TGTTTTAAAG TTAAACTATA 360 AAGTAAAACT ATAGTTAGAC TATAAACTAA AACTATAGTT AAACTATAAA CTAAACTCCT 420 CCCATAGGAA TTTAGTTTGT TCACCATGCA GGAAGGAGCA AAGGCAGTTA TCTTGTGACA 480 TCAGAAGCAA GATGAAGTCA GCTATGTTAG AGTTCTACGT TATGTATCTA CATTATGCCA 540 GGCACTGTGC TAGACAATGA AAATGTGATA AATACAATGC ATTGTGCAGC TTCCTCTTGG 600 AGCTTGTAGA TTATGAAAAG GAAATAGACA TAAAAATACC AAGCCAGTTA TTATAGAATG 660 GAAAGTATAG AGAGTTATGT CTTGGGCACC TAATTGAGGA TAAGAACCAG CGAATTTAAT 720 GTATTCAAGT ATAATAGGAT GCCTGGCAAG ATAAGCAATT TGTTCTTTTA TTTATTGCTA 780 GAAAAATCAC TAAAGTTTTT GTGCATAGTG GAAAATGCAA AGTGTCCTTC AATAATTTTT 840 CTTCTTCAGA CTTCCTTTTA CGTCACGGTT TCTTCTCAGT GTCAATGCAA TTAGGAGTCT 900 TTTTGCCTGA GGGAAAGATA CAAAAGACTC GCAGTCTGAT AAGGCTGCTG CTTCAGAGAC 960 CCTTTGCTTT ATAAAGTGGT TGCAATGGCA AGAATGCATA GTATTGCATA GTGTTAAAGA 1020 GGCTGGGGTC AGGGGGTGGG AGCTGGTGTT TTTATAAATC ATGACCCTCA CATCTTCTAT 1080 TTTTAGTGGA AACTTTATTA AAATATCTCA AATGAACGTA GATTGTTCAG AACGATATCC 1140 ACTTGCATTA AAGGCTCCAA GGACCTGAGA GAGGTTCTCA AAAGGAAGAA AGGGAACATC 1200 TTTTTGTGAG ATCCAGAAAT ATCTCTACAG TCTGTAGTTT TATCTAGAAT ATCAGTAAAT 1260 GGTTAAGCTT TGGAGTCCTT GCAGCACCAG CTACCCAGGC ATAGTGATAA TACTCCTGAA 1320 TAGTGGCTGA ATGTGGATGT GTACAAGAGT TCTAATCTCT GAACACAAGT GTGTTCAATT 1380 ATGAGACTCT AGAGCTTCTC TCTAGGTATG TGGCTCATGG 1420
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