Tag | Content |
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EnhancerAtlas ID | HS133-14423 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr19:289560-290950 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr19:290358-290369 | ATGTTTACATA | - | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_24943 | chr19:288744-291508 | Colon_Crypt_3 | SE_69126 | chr19:287282-291446 | H9 |
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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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Enhancer Sequence | AAAATTATCT GGGTGTGGCG GTGTCCCAGC TCCTCGGGAG GCTGAGGCAG GAGAATCGTT 60 TGAACTCAGG AGGCAGAGGT TGCAGTGAGC CGAGATTGCA CCACTGCACA CCAGCCTGGC 120 GACAGGGCGA GACTCTGTCT CAAGAAAGAA AAAAAAAGGG CAGCGCCAGG GCCTGGAGGC 180 AGGGCAGGAC GGCGGAGAGG GCGGGATGTA AGAACCTGCC TTCTGCTCCC ACACAGGAGG 240 GGCTGGAGCT GCTGTGAAGG GAGAGGCCTT GGAGGAGGCT CCTGCAGTTG CCGGCCGGGT 300 GGAAAGTCAG GGTTACGAGA TGCCCAGAAG GGAGTGCAGC CCGACCACAG CTCTTATCGG 360 GCGGAGGCTC ACACAGGTTA GCCTCCGTTT CCGACCTCCC TGCCCCAGCA ACTCCAACTA 420 GAGACGCAGG CACCCCCATA ACGACAGGCG CCGGGCTTCC CTCGGCCTGG AAAGCTCTCC 480 CTGGGGTCCC CAAAACAGAC ACCTTCTCTT CATTTAGCCC CCGGGAGCCC TCCCGCCCTC 540 ACACTGCCCT CATGCCAGCA TCTGGAACCT CAGTGTTGAC TGAACTGTGG TGTGCTCAAG 600 CTTCCAGCAT AGAGGTGCAC TCGGCCTGGC CACCACCCCT GGCACACAGC AGCAACAGCC 660 AACCCCATCT CGGCTGTACC TCCCGCTGCT GTGTGACCTC CGGCAGGTGA CTCAGCACCT 720 CCCTCACAGG CTGTTGTAAG GGAAATGTTT GTTATTTGCA TGTTGCTTAG TTCCTGGCAT 780 ACAGAAAGTG CCACCTAAAT GTTTACATAA ATAACACCAT AGGTGCTCAG GAAATGGTAC 840 CACGGGCTGG CAGACACCCA CAGGGACTTC TTGCTGTCAC CTGGCCCACC CTAAAAAAGG 900 GTCTCCTTCC GGAGGTAAGA GGACTTGGCC TCTGCTGTGA GATGGCAGAG AAGCAGGAAA 960 CACGTTGGGG AGGAGGGCAC CCCCCAGAGA TAGAATTCCA GGGCCATTGT CTGTGCAGCC 1020 ACAGAGCAAA CACTCGGCCT TTGTTCCCGG GACCCTGCGG GAGGGGGGCC TCGGGATGCC 1080 CATTCCGCCA GTGTGGCCCG CAAACCCGCC GGACAGGTTT GGTTCTCCTG GCCTCCCGGC 1140 CCCCCGCCAC CCCGTTCACC CGAAGCCTGG GACCCAGCCT TCATCCCCAG TGTCTCCCCC 1200 GCCCGAGCCA GCAGGGCGGC TGGGCCTCCC CGCACGTGCA CGGGTTCGAA TCCCGCCGAC 1260 GCACCGGGTG CCAGGACCGA GGGTCAGCCC TCTCCGCGCG CAGCGGGAGC GCCCACCCCA 1320 GGGGCGGAGG CGCGGACGTC CTGCCGGGGT AACCCGCGGC CGCCCCCACC TCCCGGGCCC 1380 GCGTGACTCA 1390
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