Tag | Content |
---|
EnhancerAtlas ID | HS133-04057 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr1:247802140-247804250 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr1:247802768-247802779 | GGGGGCGGGGC | - | 6.02 | KLF4 | MA0039.3 | chr1:247802327-247802338 | CCACACCCTCT | + | 6.02 | KLF4 | MA0039.3 | chr1:247802268-247802279 | GGAGGGTGTGG | - | 6.32 | KLF5 | MA0599.1 | chr1:247802769-247802779 | GGGGCGGGGC | - | 6.02 | ZNF263 | MA0528.1 | chr1:247802733-247802754 | GGAGGCGGAGTGGGAGGAGCG | + | 6.09 | ZNF263 | MA0528.1 | chr1:247802393-247802414 | AGTGGAGGAGGGAGAGGGGCA | + | 6.27 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCAGGAACT GTGCTCCTGG GTCCTGATAC CAGTGCCCAG CCCATAGCGG GGGATCCCCA 60 TTTTATGATA AGAATAAATG AGCACCTCCC AGATCGGTGA CTTGCTCCAC CCCACAATAA 120 CCCCGGGAGG AGGGTGTGGT CAGTCCAGCT GTACAGGTGA GAAAGTGAGC TGGGAGCTGT 180 GACTTATCCA CACCCTCTCA GCAGCAGTTG TGACAGCTGG GGTCACACAG TTGATTCACT 240 GCCATAGGGG AAAAGTGGAG GAGGGAGAGG GGCAGAGAGC GAAGAACAAC TCAGGAAAAT 300 GAAGGAAAAG CAGAGGCAGA GAGCGAAGAA CAACTCAGGA AAATGAAGGA AAAGCAGAGG 360 AGAAATTAAC TGACTGGAAA AATGACAATA GTTGGAAGAC AGACGAAAAA GGGACGAGTG 420 CATCAGAGTG TATTTTGGCA CTTATTACTC TATCTCCTTT TTATACTACT TCGCTTTTTC 480 AACTTAATAG TTAAGGCACG TCGGTCTAGT CTTCCCCGAA GGGAGCTTGC CAGGCTCTGC 540 GACAGGCTTG GAAGTTGGAG CCCGGGCCCT GGGTTCTCTC AGCTTCCAGC TCAGGAGGCG 600 GAGTGGGAGG AGCGGGCCTG GCGGCCGTGG GGGCGGGGCT GCTCCACTAA CGGTTACTGG 660 TCGCTGCTGC CGCCGCGCTC CTCCCCCGGC TGCGGCAGAG GCGCGCGCCT GCGTCCTGAG 720 GATCCCGCCC TTGGGCCGCC GGGAACCTCG CAGAGCGGCG GGGTGGCCCT GGCGAGGCGC 780 GGTTGTTGGG GGTTCGCTCG AGCCTCACGA CGCCCGCGAC TGGGGACTCG GAACCTGGGC 840 CAGGCTGGGA CGAGGCCGCG CGGGAGGGCG CGCTGGGCGG ACGCTGGGGC CGCGGAGCCC 900 AACCGCCCTT GTCCTGGACG CCCCTTGGCG GTCCGCACTG GCGGGTGCCC TCTCCCGAGG 960 GGAACTGAGG CGGGGCGCCT GCCACCATTC GTGATTTTCC GTGACTCACC CTCTCAACAG 1020 TGTCCCGTCA GCCCCCGCTT TCTGGAATTA AGATGATTTT CCATGGGCAT TATAGTCAGA 1080 GGAGGTTTTC TGTGAGACAT CTGGGAAAGG TGACTCAATG ATCACTCATA TTGTTCTATG 1140 ATGTTATACA TTTAACCGGA ATACTGGTGA ACAGCTTTTA TATCTTGGAA TTTTTTCCCA 1200 TTTTTGAATC AGAAATTTAG GACCAAGAAT CTTCTGTCAC AGAACCTATT ACTTTGAGGA 1260 GTGAACTTAT ATTAACGGTG CTAAACCGTA CATGAACGAC TTGGTAGATG AAAACTTTGG 1320 AAAATAGGAA CATTTCATGT CATCACATGT ATCCTCCAGC ATTGGGGAAA ATTCAACAGT 1380 TGCCTTAAGG CGGGAGTTTA ATTGAGGACA TTTACTAAAA AGTTACTTAT TCTGTTTGAA 1440 ATTCTCTTCT GATAAACATC TTCCCGGGAT AACGAACATC TCCAGGATGT GAGAGCCGAG 1500 CGCGTGTCCG CGGAGTGCTT GAGCAACGCA GAATGGCTTC GGTGCTGCGT TCCTTAGACC 1560 CCGTGCGGAC CCTGCTGAGC CCTCAGCATC TGTGAGTGAG TCCCTCCGCG TCACCTTGGC 1620 CTCCCGTGTA GCTAGATCAG TCTTCCGACC CCTTGTTCTA CTTGCACAGA TTTCTGATTA 1680 ACCTCTTCTG CTCCTCCAGA GATGAGTCAG GGCTCCGTAT CAGCTCCCCA AGGCATTTGC 1740 TGGCTTCTGA CATTTACTTG GAGGACTTTG GGCTGCGAAA GGGCAAAGTT TGCCGTTCTC 1800 ATCTCTTTTT TTGGTGCCTG CCCCCGGGTC TTGACCTTTC TCTGGAGTCT TCTCTCCTGG 1860 TTCTTTACCC ACCTCTTTGG TTTCTCCTGT GGTTCTTTGT CAAGGTGTCC CCTAGATGTC 1920 ACACTCTGAG GCTCAGTTGT GGCTGAGTCT TGCATTGCAA GTGTTTTTGC AGGTGTCTCT 1980 GCGAAGCGTG GATATGGGAT GGTGAAAGTG GCAGTGTGCA CAGAGTGTTT GGGATTAGAT 2040 GGGCAGGTGG AAGGGCGTCT AGGTAGGACC CCTTTGTCCT GGTGTGAGGT AATGAGGTTC 2100 TAGAGTGTGC 2110
|
| |
|
|
|