Tag | Content |
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EnhancerAtlas ID | HS133-18411 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:242620100-242621270 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr2:242620438-242620449 | GGTGACTCATC | + | 6.32 | JUND | MA0491.1 | chr2:242620438-242620449 | GGTGACTCATC | + | 6.62 |
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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 |
GH02I241678 | chr2 | 242618303 | 242622569 |
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Enhancer Sequence | GAAAATTATC CCAACAATAC AACTCAGAAA TCTCATATGA CAACAAGTAC AGCACAGTGA 60 TTTGTAACCT TACTTTTAAT CCAAAAAGGT CTGGATCTTC TCTAGAAGAT GCCATACCCA 120 CACCTCCAGC AAAACCCAAC ATGGAGAAGA TAACCTTACT AAATAGTAAC AAACACAACT 180 GGTAAAGTTC AATGTTCCAG AAACACGGCA GGGGAAAGGA GATGCACTGT CAGCTGTCTT 240 GGTCAGAGAG GCCAGCTCTA CCCTGTCGAG GAAGAAGAAA GCACAGGCAA AGAAGAGAGC 300 AGAGGATGGT GGCGGGGGAA GCGTGGGCAC AGCCAGCAGG TGACTCATCC ATGCTCATGA 360 CCCCTAGCCT GGACTGCAAG GATGTTCTCA GCCAAATACC ACAAGTCCAC CATCATCCCT 420 ACAGCTGCCA AGATCACAGA TGTACAAAGA CACGGGGCCT GACACTAGTG AGAAGCACTG 480 CTCAAGACAG AGAAAGAAAA GTCCGATTCA TTCGACTCAG CCAGTCTCAC TGGGGCCTTC 540 AAATCACAGG GGCACCCACA TAAGGAGTCA ACTGGCCTCT GACAAAGCAG CAGAGGGATG 600 CAATGGTGCA AAGGCATTTT CCTCAATAAA CGCTGCTGGA ACAACTGGAC ATCCTCATGA 660 AAGAGAATAA ATCTAGACCA GACCGTATAC CCTCCACGAA CATAAATTCA AAATGAATCA 720 CAGGCCTGGC ACGGTGGCTC ACGCCTGTAA TCCCAGCTTT CAAGGAGGCA GAGGCAGGAG 780 GATTGCTTGA GCCCAGGAGC TCGAGACCTG CCTGGGCAAT ATAGTGAGAC CCCGTTCTCC 840 ACAAAAAGTG GGGGAAAAAA AAGACAAAAT GAATCACAGA CCCAAATGTA AAATGCAAAA 900 CTATGCAACT CCTAGACAGT AACACAGGAG AAAACTTAGA TCACCTGGGG TTTGGCAGAC 960 TGTTTAGATA CAAAACCAAA GGCACAGCCC ATGAGAGAAT TGATTAAGAT GGACTTCACG 1020 AAAATAATAA CTTTGTGCTT TGTGAGAGAC ACTGTCAAGA GAAGGAAAGG ACAGCCGGAC 1080 GTGGTGGCTC ATGCCTGTGA GCCCAGCACT TTTGGAAGCC ATTTGGCGGG ATGGATCCCT 1140 TGAGGCCAGG TGTTTGAGAC CAGCCTGAGT 1170
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