Tag | Content |
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EnhancerAtlas ID | HS133-02131 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:117188100-117190060 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr1:117189630-117189641 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr1:117189630-117189640 | AAAACAAAGG | - | 6.02 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I116645 | chr1 | 117188405 | 117192183 |
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Enhancer Sequence | TGGTGAGTTC CGTTGTATGT AAGCAAATTA TACCACAATG AAGCAAATCT TTAAAACACT 60 AGGTTCCTTT TCCTTATCTA GAGCTCAAAG TAGTGGCCCA TGCTGGCTAT GACTTGGAGA 120 AATCACATAA GCTTACTGGG TCTCAACTGC TTCATTTGTA CAGGTGGCTG CATAACACTC 180 CCCGGGCAGG GGAACTGTAG GGAGGAAATC AGAAAATGTG AGTGAACACA CAGAGCAAGC 240 AACACATAGG CCTTCCCCAA ATATCCACTT CTGTTTTCTT TCCTCAGTGT GAGTAAGTGG 300 CTCTAATGAT CCACAAACCT TCCAACCAGC CAAGTCAAGG ACCAGCAGGA GGACTCAGGA 360 AAGTACTGAA ATGCTGGGGA GAACCAGGAC AGCGGCTGAG CACAGCCAGA CAGGGAGGGC 420 AGCCTGGTGG GGCCCTGGAA GCCATGGACG CGACTGCGCT GGGAGTGGGG ATGGGAGGTA 480 GCAGGAGTTG GTGGGTGGGG CACAAAGTGG GAGCCAGGGC CGAATTGCTG CTGATTTGAC 540 CATTTTGCAA AAGGCCAGCC TGGCTGTGGC CTCAGGCCTC TCACTTCCTC TACCCTAATG 600 AGGGGTCATA GAAGTGCCTT CCCACAACTG CAGCATCTCC CTCCACATTT GGGCTCAAAT 660 ACAGAGTGGG GCCGGAGACA GAAAAAGTCT CCGTGACACA CTGTGATTTG TTTCTGCACC 720 GTGTGAACCC TTGGCTCTGT GACACGGAAC ACAAGTTTCA GCAGTTCCTG TCACTTCCCA 780 CAGGCGAAAC AGACAGAGCC TTCTTTTGTC CGGCTTCTGG TGAAACGCCA TTATCGTTAT 840 TTTTAGGAGG AAGATGGAGA ATTGGGGGGG GTCCACACAA AGAGGATGGA TTCAGAAGAC 900 TTCCAGGAAC CTTAAAAGCC TTGGAAACTA ATTGTGCCAG TTCTTTTTGA TGTCTAATTT 960 TACTCCAAAA GTTCCTCTCA GCACAATATA TTAATACTTA TCAGCCAAGA GAAGGTTAGG 1020 TTTTGGCTCA CAAACAGTCA AGGAGAGAAT CTCCTTAATT CATTGAGAAG GCAGAAGATG 1080 GCGTTAAAGA GTATTCATAG GTAACTAAGA TTGCCAGAGG GAGAATCGAG TGAGTTGTCA 1140 GCGGTGAAAT ACAGAGGAGG TAGAGAGAGC TACACTGAGA CAACAAAGGC AGCTTAAGGG 1200 AACAAAGCCA GCTAAGGGAA CAAAGCCGGG GTCCCTCAGG TCTGTGGCCA CCGGCTACAG 1260 CCAGGACAGC CTGGTAGCTG AAGAGCACGT CCTTGCCTGT TACATGCCTG TGTTTCAAGT 1320 GATGCTAACT TGCTAATGCA GATGTCTCCC CAAACCCTGC CCCTGGCTCA CCACCCAGTG 1380 AGCAATCACT CACTTTCCCC AGGACACCTT CAGGGAGGTA CTCTGCCAGC ACCGCACACT 1440 TAAACGGCTA ATGCAGGTTC TTCTCTCAGA CGCAGCACAG TTCCTGAGAT GACGTCAGCG 1500 CTGCTTGCTG AAAGCACCAG GCAAGGAGGC AAAACAAAGG AAATCCTAAA GAGCAGGCGA 1560 GAGAACAGTG GAACTGGCAG AGAGAGGCAC TGGTGCAGAT GGAGAGGGCA GCAATAAAAA 1620 CTGGGGGACA CTTAGAGGCA AAGGTATGGC AGGTGACAAA AAAGATGAGG CTGAAGGTCA 1680 GGAGAGACCC AGGCAGCGAT GCCCAAATGA CCGGCTGAGG AATCACCTCA CTGCTGCCGA 1740 TGCCCTTGAC AGCGATGTCT GAGGCTGGCG TGAGTGCTCC ATGCTCAGAG ATACCTAGAA 1800 CCCAGCTACA ATGGCCTTAT CAGACTGAAA CAAGAACACC AAGATATTCC AAGGGAGGTG 1860 ACAATGGGGT CCAAAGGTCG TGCCTTTATG GCTCGCAACT ATGTGCTGAG TGTGGCCCAA 1920 ATTCCAGCTC CAAATGGTCA CACCATGTCT ACAGCCAATC 1960
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