Tag | Content |
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EnhancerAtlas ID | HS133-12141 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:1914670-1915880 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr17:1915858-1915879 | TTTTTCTTTCTCTTTTTCTCC | + | 6.22 | NFIC | MA0161.2 | chr17:1915504-1915515 | TCTGCCAAGTA | - | 6.62 | STAT3 | MA0144.2 | chr17:1914728-1914739 | CTTCTGGGAAA | + | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_08640 | chr17:1914316-1915669 | Brain_Inferior_Temporal_Lobe | SE_41649 | chr17:1914573-1915947 | LNCaP |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 1914714 | 1915703 | chr17 | 1915709 | 1915808 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I002010 | chr17 | 1914201 | 1915923 |
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Enhancer Sequence | ATGGTCTGTA ACACGGTCCG ACAGGAGTCA TGACACGGCT GGCTCCACTG GGCTCTTCCT 60 TCTGGGAAAG CCAGGAATTG GAGGCACCTA GCTGTGGGAG GGGAAGATGA AAGGCCGTGC 120 TGGAGAGCAA GGGGTGGGTC CATGGCTTTG GATGTGGGGC AAGAGGAGGA GCTGGCGGGG 180 TGGAGGGAGA GGCCAGGGCA GAGAGGCCAG GAGAGGGACC ACGGAGGGCT GTACATTCTG 240 GAGCTCCTCC CTTGCCTGGA GGCTTTGGGA GTCCAGGTCA CTCATCTCCT TGCAATAATC 300 CCCCATTTCC AATGAGCTCC CATGAATCTC TGCAATCAGA ATTGGCCATG AAAGCAGAAA 360 TACCAGCCCA TCAGGGGCAG TGGGCCAATT AGGTAAGATG ATCATTGCCA CAATCTCAAG 420 GCAGCCCCGG GGCTAACTGC CACCCCACGA GTCACGTGTG AGTGGTAAAA TGTCCCCTTT 480 GGCTGGTGCA TTCTCTTGAG CATAGCCCAA GAAGTTCCCG AGCCTCTTTC CCTCGGCCCC 540 TCCTCGCTTG GGGAGATTCT TTTTAAACCG CAGGCCTGAG CAACGCCCCT GGAGCCCTCC 600 CTGGGAGGAG AGGAAGCAGT TCAAAGTAAC GAGTCAATTT CACAGATGGG AGCCAAGACA 660 AAAGAGGCAG CGTCTTCTCA CCCCAGGCAC CACCCGAGCT CAGCTTCCTC TGGCAATTTT 720 AGCATGTTTG GTCCGGCCTC ATTTAGACAT TTCAGATCTC TGAAGCCCAG AGAGTGTCCA 780 TGAGAGGTTT CCGTTTGCCA CGGAGTCGAT AGTACAAATT TTGTTCCAAA CACATCTGCC 840 AAGTACAACC CTAAACTTTT CCAAGCGAGA GGTTATTTTC CTAACACAGC GCCTGCTCTG 900 CTGGGCATCC TCTGTGGTCC AGAAGGCCAG TCTTTCCGTG CCTGCTGGCT TCCTGGAGCC 960 ACAAGGAACA CAGCTGGGCT GCGGTGAGGC GGCCCTAAGG CCCTGCCCAA GCTACTGAGC 1020 CCCTCAGAGC CTCGGTATCC TCATCTGTAA CTTGGGACTA ATGAGACGTG CGTTTTCTGC 1080 TTTTAATGAG GCATTGCACA GGGAAAAGTG CGTGGTGTAG GACTCTTCTC TGCATCCTCC 1140 TCACTAAAAA TTCCCCATTT CCTCCTGGTT CCTGGTACTG TTTCTATTTT TTTCTTTCTC 1200 TTTTTCTCCT 1210
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