Tag | Content |
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EnhancerAtlas ID | HS133-17855 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:177507300-177508840 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr2:177508295-177508305 | ACCAACTGTC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 177508502 | 177508600 | chr2 | 177508506 | 177508706 |
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Enhancer Sequence | CGCCACTGCA CTCCAGCCTG GGCGACAGAG CGAGATTCCG TCTCAAAAAA AAAAAAAAAA 60 AAAACTCCAT CCAAGGATAA ATTTCAAAAG TAGATGCTGA AAAGATGGAA GTCACTGGCT 120 CCACCTGGTA AATCCTATAC TATCCCTGAG AAGGCAGAAG TCATTCTTAG GTTTAGAGAG 180 AGTCTACTAC AGCCAAAACA GTTAGAATTA ATCTTGGACT TATGACTTTG TGGCTGTTAT 240 TGCTGGGACA GGGGGACGGA AATGGGGGGA GGAATTGAGG GATACCTCCA AAGAACTCAC 300 AAGTCTGCAG AGACCGAGCT CACTACATAA ATACAGCAGT GGCAGACTCC AAACCTCAAC 360 TTGCTGCTCA GGGAACCCCA GGCAGTACCA GGCTTTGGTG GCTTTGCTGG AAAAGAGTTC 420 TGGGGTTTAC CAGCCCTCTC ATGCATTTAA CTCTGGGCAC TCAACTCACC TTAAGTCTTT 480 GAGTTTTCTT ATTGAAAGAG AAAAGTAATC ACACCTTAAA TTAAATTTAT GGGTTTTTTT 540 GAATAAAGGA TATACTTATA GTTTCCAGCT CTTCACTGTG AAGTCTGATT AATTTTTTAA 600 CAGATGAGGA ATTTGTGTAT TGATGAATAT TTGATAAAAA CAAGAGAAAA CATTAAAAAG 660 CAACATGAAC TGCAGAGTTC AATCCCACCA AAATAAAAAT GTAGCACTGT ATATCTTGAA 720 ACTGAGGTTA GACTCTCTAG GAAGAACATG GAGGAAATAA ATGCTCAATC CATATTGCAG 780 CAGACATAAT TTTAAGCCAC CACAACTTTC AAGGACCTTT GAACCATTTT CTTCAAATTT 840 GCCTTGCCTT TCTTTCTGCA TCTGTGAACT TGCCAAGTTA GAGTTTATTG CTGTAACAGG 900 TTTTGAATGA TAGTGTATCT GTTTTGAAAA GGTCAGTACT TTTTGATTAT TTGATGGAAA 960 GAATGTGTGC TTTTCCTTTT TTATGTATCT TTCAAACCAA CTGTCTTGAT ATAAATGGAA 1020 TCTTTAAAAA ATATATTTAC CCTTTTTAGA CTAAGACCAA ACATTCCGTT CCATGAAAGT 1080 CATGAGTGGT TGCTGAAAGG AGGTTATGAA TGAAATAGTG TCTCCGCTTG AACGTCAGCA 1140 GCTAGCCTGC ATTTATTCCT CAATTTCCAG AATCTAGAAT AAAAATAGTG ATTAGCAAGG 1200 CCAAAATACA AAACCCCAGG ACGTAAAGCA GTGAGCACAG GGAGGCTCCC AGGACAGGAA 1260 GCCACTGGAA GCTGGTTGCT AGGAGACACT CGTCTTTTGC CGGCAGCAGG AAGATGTCCT 1320 TGAGCATGGC TTCCCCTGTG GTTGGCTTTG GACAAGCCGT GAATCAGACT GTCCTCACTA 1380 GTGCCGCCCT CCCAGCAGGG CCGACCAGCC TACCATACAG GTGCCACTGA GGGGCAATGG 1440 TGGGTCCTGT TCCCTGGGAA AGTTTCTCAC ATGTGCCCAG CTTTTCTGAT ATGCTCTTCT 1500 GAAATCAACA AGCATTTGAT GTCTACTCTG GGTTATAAGA 1540
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