Tag | Content |
---|
EnhancerAtlas ID | HS133-26950 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:39368980-39371600 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr6:39370911-39370929 | CCCTCCTGTCTTCTTTCC | - | 6.16 | GFI1 | MA0038.2 | chr6:39370163-39370175 | TGCAGTGATTTA | - | 6.92 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I039402 | chr6 | 39369791 | 39370816 |
|
Enhancer Sequence | AGGCCAGTAG CCTTTCTGCA GTTGCTCAAG TCACTTTGGT TGAGAAAGCC TGCATAATCC 60 AGCTCCCATT TTCCTCTGTC TTCTTTTCAC CATCTGAGTT ATCTCAGAGG TAACACCCCA 120 TACCCCCTAT CTTAGTGTGG TTTCTCCTGG AAGCAGACCC TAGTACAAGT AGTTTATTTG 180 GGAAATGATC CCTGGAAGCA CTGGTAACAG ACAAGGGAAG TGAGACATGG AGGGAAGGCA 240 GCCAATCTAG GGGGCAATGG CAAGCCATTT TCCACTATGG GCAATTGGAG CTCAATCCCA 300 CTTGGAGACT CTAGGGGCCT GTAGAGGATA CATGCCTCAG AGCTCTCACT CCTGCAGAGG 360 GAGGGAGCTG GGGTACGTAT ACACCAACTG CCAACAGTCA TTGATTGAGT CCTCCCGGGG 420 CAGGGGATTT TAATTCCCCA GCACCAGCCT GCCCCACATA TATCTCTTGA GTAGGTGAAA 480 AATGCTCTCG GGGGAGTGGG TAGTGCTAGC AGGTGAAGTC ATGCTAGTGT GCACATGCCT 540 GGCATGTGGA AGGGATGCAG GTGGGGCTCT GACAACATCT ACCCTGTTCC TTATTTCTTG 600 TTTTTCATTA TCCTTGTCTG AAAAATATTA CTACTGCCTG TAGTTAATAT AGTCTCTTAC 660 AAACAAACCT AATTCTTTGG CAACAAAACT AGCAGAGAAA GAGGCAGAGG AAATGAAACA 720 TTCTAGCTAG TCTATTGCCT GATTTCTTAT AGGCCTGGCT GGTATTTTGG GAGTCAGGTT 780 TGTTTTCTGG CCTGGCAAAT AGGAGTAACT GTAGCAGCCC TTGGTTTTCT ATGGACCCTA 840 TTTTAATAGA ATGCAGACTG CTTAGACTTT GGCTCACATT CTGCATGCTG AGGTGAGCTA 900 CTCTTTCCTC ACTTGCTGCC TCAGTTTCCC TTTTTGCAGT GACACCTCAG ATAGGAAGCT 960 CTGACATCAG AAGCTCTTCA ATTCAGCTTC TACTTGGGGC AATGGAAAAG GTACGATGTG 1020 TTACTGTGAT GGAAAGCACT GTCAACCAAC CCTGGCAGAG GTGCCAGGGG CATGAGGGAC 1080 TCAAGCCGTT TCGAGGACTC ATCCTAGAAC AATGCAAACA ATTGTCCTCA ATCCTGGGTC 1140 TATGGGCCTG TTTACTCACT CCGTGCTGTG CCCGGCAGAA ACTTGCAGTG ATTTAGGAAG 1200 TCAGGGAGAG ACATTTCTGG CTGTGCGGAA CCTGATGAAA TACTGTTTTG TGGAGACAGA 1260 CTAAAAAATA ACCAAACGGT CTTTAAGTGG AACAGAGATC AGAAAATCTC CTGAGGCACA 1320 TTTAAGAAAC CCATCAATTT TGCTGGCTTG GCCATAGAAG GGAAAATTGC ACTGCAAATG 1380 ATTATCTCTG ATGAAATGTT CCCAAGTCTT TTACAGGGCA CTTATTTGTA GTGACCTATT 1440 ACTCCACCAA CGAGGCCTGA CTGAGAAGCC CCCACTGGGT GGTTTATAAG GGGAGTCTGC 1500 AGAGTAATTG CAGGCTCAAT CCTGAGGGCC TCCTGTGTCC TATCTTCTCA ACCACCTTAC 1560 AGGTATCCTG AGGCTGGGGA CTCTCCTATG GATTTGTGTG TTTTCCACAG GGCCTCCAAC 1620 TTTACAGATG TACATAAATT ACTGAATGAA TAAACCTGAG ACCAAGGCTT TCTGCCCAAA 1680 GTCCTCATCG TAGAAGCCCT CAATTTCCTA CTTGCCCTGA CCAAACTGAG GAAAAGCTGT 1740 GGCAAAAGCT CCTACTGCGT TCAGCCTGAA ATAATTCACC ACAACCTGTA TCATCAACCC 1800 ATACCCAATT ACCTAAAGTG CTCTTTCTAG AGAAATTAAA AAAAAAATTC TGTTCTCCAA 1860 CATAAGATTC ATTTTAAAAT GACAGCTGAG GTCATTTCTT TTATAAAAGC TGAGGTGGGT 1920 TGTCTGATAT TCCCTCCTGT CTTCTTTCCT TGGTGGATTC ATACTGTTTT ATTTTTTATT 1980 TATTATTAAA TATGGTAAAA TTGACTTGGG AGCATGTGTG TGCATCATGG GTTTGGACAC 2040 ACACATAGAT TTGTGTAGCC ACCTTCAAAA GCAGGATCCC CAAGAGTTCT GTCACCCCTG 2100 GACTCCCTCA CAAGGCCATG TTGGACTCAC ACCCTTCTCC CACCCCTGCC CTGCATTGTG 2160 GAAGTTCTCA CTTTTTCAGA ATGTCATATA GCTGGAATCA GATAGTAGGA GGCTTTATGA 2220 GACTGGCTTC TTTCATCCAG CACAATGCCT TTGAGAGTCA CTCATGTTGT CTTATTTACC 2280 AGCAGTCTGC TCTTTTTATT GCTGAGTAAT GTTCTATTGT ATGCACTCTA TTGAAGTCTA 2340 TCCCCTCACT CACTGAAGGA CATTTGGGTT ACCACCAGTT TTTGGCAATT ATGAAGAGAA 2400 CCCTTACAAA CATCTGCATA CAAGTTTGTG TGTGAACCTA AGTTTTCATT TCTCTAGGGT 2460 AGGTAGTTGG CTTGTATGGT ATGTCTGTTG AATTTTGTAA GAAATGGCCA AGTTGTTGTC 2520 CAAGGTGTCT GCCCCATTTT GCATGCTGAC TAGCAACATA CAAGAGTTCC AGTTGCTCCA 2580 CATCCTTGCT ATTACTTGGT ATTGTCAGTT AAAAAATTAA 2620
|