Tag | Content |
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EnhancerAtlas ID | HS133-02690 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:160915080-160917710 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:160915824-160915835 | GGTGACTCATG | + | 6.62 | FOXP1 | MA0481.2 | chr1:160916597-160916609 | GAGTAAACAGAA | + | 6.27 | IRF1 | MA0050.2 | chr1:160916506-160916527 | AAAAAAAAAAAGAAAGAAAAG | - | 6.41 | JUND | MA0491.1 | chr1:160915824-160915835 | GGTGACTCATG | + | 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 |
GH01I160946 | chr1 | 160916587 | 160918989 |
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Enhancer Sequence | TGCTGGGAAA CAGAAAGAAG AAACACTGTG AGGAATTTGA TTTGCTGCTG ACACCAGTGA 60 GCGCAAGGCT GGTCTCGAAC TCCAGACCTC AAGTTATCCG CCTGCCTCGG CCTCCCAAAG 120 TGCTAGGATT ACAGGTGTGA GCTACCACAC CTGGCCCTAT GCATGTATTT TAAAGTAGTA 180 ATGCATGCAG GAACATACAC AAACACGCAC TAATGGACAG TCTGAGGAGC ACAGAGCCAG 240 TAGAGAAACT TGTCAAGGAA AAGGGCATAA AGACATATAC TCTAGTCCAC CCCCACTGCC 300 CACGTGGTCG TCATCCTCCG AATTCTAATC TGCGAGTCCC TCCATGAGAG AATAGCTGCC 360 TCATCTTAGC TGGAAAATGA AAAAGCTGAA AGCTGGGGCA GGGAAGATGG AACCGTGAGT 420 TCAGACTGTC AGTTGGGGAG GGAAGGGGGC CCTAAGTGAA TGCCCTTGTT CTTGATGGCT 480 CTGACGCTCT CTTCCTCCAA CCCCTAGGCA CAGGATGTCC CTCAAATACA ATCTCCCACC 540 ACTACAACTG TGGTGCTGTC TCCTACAAGA CTGGAAAAAC AATAAAAATA TAAAGCTTCT 600 AAAAGTTAAG ATTAATATTG GAGAATATTT TCACGACCTC GGTGTAAGGA GGTACATCTT 660 AAAGAAAACA TTAAAAGTAC TAACCATAAA TGAAAAGTTT GATAAACTGA ATTCCATTAA 720 AATAAATTAT ACTCAGCCGG GCACGGTGAC TCATGCCTGT AATCCCAGCA CTTTGGGATG 780 CCAAAGTGGG CAGATTGCCT GAGGTCAGGA GTTTGAGAAC ATGGAGAAAC CCATCTCTAC 840 TAAACCCATC TCTACTAAAA ATACAAAAAA ATTAGCCGGG TGTGGCAGTG CATTCCTGTA 900 ATCCCAGCTA CTCAGGAGGC TGAGGCAGGA GAAACACTTG AACCCGGGAG GCAGAGGTTG 960 CAGTGAGCAG AGATCCTGCC ATTGCACTCT AGCCCAGGCA ACAAGAGTGA AACTCCCTCT 1020 CAAAAAATAA ATAAATAAAT ACATAAGATT TAAAAGACAA ATAAATTATA CTCAACTTCT 1080 GGCATCTACT ACTCCAAACT TTGTACCACT TAATTTTTAT TAAAAATATG GACTCTTCAG 1140 GCTGGGCGTG GTGGCTCACG CCAGTAATCC CAGCACTTTG GGAGGCCGAG ACGGGCGGAT 1200 CACGAGGTCA GGAGATCAAG ACCATCCTGG CTAACATAGT GAAACCCCGT CTCTACTAAA 1260 AATACAAAAA AAATTAGTGG GGCGTGGTGG TGGGCCCCTG TAGTCCCAGC AACTCGGGAG 1320 GCTGAGGCAG GAGAATGGCA TGAACCCGGG AGGTGGAGCT TGCAGTAAGC TGAGATCGCG 1380 CCACTGCACT CCAGCCTTGG TGACAGAGCG AGACTCTGTC TCAAAGAAAA AAAAAAAGAA 1440 AGAAAAGGAC TCTTCAAAGA AAAAAAAAGA AATAAAAAAT AAATTATATT CATAAGACAT 1500 CATCAGGAGA GTAATGAGAG TAAACAGAAT GAGAGTAAGC GAGTAACCAC AGAGACACAC 1560 ATTGATACAC CCCACACAGG TACACACATG TGCATACCCA TGCACACACA TGGTGAAGGG 1620 GGCCAGCCCC TCCACATCTG TGGGTATTTC TCGTCAGGTG GGATGAGAGA CTGAGAAAAG 1680 AAATAAGACA CAGAGACAAA GTATAGAGAA AGAACAGTGG GACCAGGGGA CCAGCACTCA 1740 GTATACGGAG GACCTGCTCC GGTGCCAGCC TCTGAGTTCC CTCAGTATTT ATTGATCATT 1800 ATTTTTACTA TCTTAGTGAG GGGAGTGTAG CAGGGCAACA GGTAAGGAGA AGGTCAGCAG 1860 GGAAACATGT GAGCAAAGGA ATCTGTATCA TGAATAAGTT CAAGGAAAGG TACTGTGCCC 1920 GGATGTGCAC ATAGGCTAGA TTTATGTTTC TCTTTACCCA AACATCTCAG TGTAGCAAAG 1980 AGTATCAGAG CAGTATTGCT GCCAGCATAT CTCGCCTCCA GCCACAGGGC GGTTTTCTCC 2040 TATCTCAGAA TAGAATGAAT GGGAGTGGTC AGCTTTACAC CCAGACATTC CATTCCCAGG 2100 GATGAGCAGG AGACAGAAGC CTTCCTCTTA CCTCAACTGC AAAGAAGCCT TCCTCTTTCA 2160 CTACTCCTCC TCAGCACAGA CCCTTTACGG GTGTCAGGCT GGGGGATGGT AAGGTCTTTC 2220 CTCTCCCATG AGGCCATATC TCAGGCTGTC TCAGTGGGGG AAAACCTTGG ACAATACCCA 2280 GGCTTTCTTG GGCAGAGGTC CCTGCGGCTT TCCGCAGTGC ATTGTGTCCC TGGTTTATCA 2340 AGAATGGAGA ATGGCGATGA CTTTTACCAA GCATACTGCC TGCAAACATA TTGTTAACAA 2400 GGCACATCCT GCACAGCCCT AAATCCATTA AACTTTGATT CATTACAGCA CATGTTTCTG 2460 TGAGCACAGA GTTGGGGCTA AAGTTACAGG TTAACAGCAT CTCAAAGCAG AAACAATTTT 2520 TCTTAGTACA GATTAAAATG GAGTTTCTTA TGTCTTCCTT TTCTACATAG ACACAGTAAC 2580 AATCTGATCT CTCTTTCTTT TCCCCACACG TGGGCCATTG ATCTCCCCAA 2630
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