Tag | Content |
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EnhancerAtlas ID | HS133-16615 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:29450550-29451660 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr2:29451452-29451463 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr2:29451452-29451463 | GGGTGACTCAG | + | 6.02 | RUNX1 | MA0002.2 | chr2:29451382-29451393 | AAACCACAAAC | - | 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 |
GH02I029228 | chr2 | 29451241 | 29451390 |
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Enhancer Sequence | CCAGAGCAGA GTTTAACATG GGGGGTGGGT GCCAAAATCT TAACACACAC ACACGTCAGT 60 GGGGCATGCA GCTCTGGCCA AAGTTAGGGG GTCACTGGGG ACCTCAGGGG CAGGGATGCG 120 GGGAGGGAAG GGAGGCTCAG GGCACAGAGG CTGCATGTGG GATTTGGCTC AGTAGATGCT 180 GGGTGTGTGG CTAATTTCCC CTCAGGTCCA GGCCAGCTCC CACTCTGCCG GTGGCCCACT 240 AAGAAGTGGT TAATGTGAGC AAGAGTCCAA AAAGTTCTAG TCTTTCCAGG CTGGGATATG 300 CCCATGGTGC CTCTCCCAGG ACTGGTCAGG ATGGTAGCAC TGAAGAGTTG CTCTTCAGCC 360 CCATTGGGTC AGGGTTGGGG TGTGGCGGGC TGTGCGGATT GCGGGAAATG AGCCCCTGTG 420 CCCTGAGGCT CCCGTCCCTC CTTTCATCTG GGGCTGGGCT ATCTTTGGGC TCCCCCCTCG 480 GGCTCCTCCC ACCCACCCAG CTTGGAAAAG AAGAGCATGT GGTTAACACA AGCATCTTAC 540 ACACAGCGTC AATGCAAAAC ACAGACACGA ACACCACAGA GCATGCATGC ATTCGTCCTA 600 ATCTGTGGGG AGCGGGGAGC CATCGTCTCC CAGCCTCTCA GCTTCAGAAG GCTCTGCTGA 660 CTGTGCTCTG AAGCCCAGAC GAGGCAGCTG GGGTCAATGG GCAGCTGCTT GCTGAAGGGC 720 TGGGCTAAGC CTGCCTGCAG TTGCCCTCGG GAATAGCTCC CATCAGCAGG CACAGCGGCG 780 CCTTTCAGGA AGCTGGTGGG CTGAGGTAGG GAGCAGGAGT AAGGAGTCCA TGAAACCACA 840 AACCAGCCCC TTCAGGAGCT GGCTTGGCCA GGCCATCCAA GGGAGGCTGG GGGAGTCCTT 900 ATGGGTGACT CAGAGACTAG TCTGGCAAGC CAAAGCCTCT TTATCATCGA CTTTGGGGGA 960 CATCAAGAAT CACATGGGAT CTTGATGCTG TCGCTGAGGA AGCCTGGAGG CAGGGTGCTG 1020 GCTCGAAAGC CAGCACCCTG CCTCTGGCTG GTCCAGGCAG GTCGAGAGGG AGGCGTGCAG 1080 TCACATCACA GTCCACACTT GGGCAGGCCA 1110
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