Tag | Content |
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EnhancerAtlas ID | HS130-12195 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr19:2395430-2396530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chr19:2396226-2396242 | CTGCCTTCGAGGAAAA | + | 6.05 | Foxd3 | MA0041.1 | chr19:2396005-2396017 | AAACAAACAAAC | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 2396000 | 2396225 | chr19 | 2396190 | 2396418 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I002393 | chr19 | 2393927 | 2396540 |
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Enhancer Sequence | AAAACAAACA AGGCCGGGCG CGGTGGCTCA TGCCTGTTAA TCCCAGTGCT TTGGGAAGCC 60 AAGGCTGGCG GATCATCTGA GGTCGGGAGT TTGAGACCAG CCTGGCCAAC ATGGAGAAAC 120 CCCATCTGTA CTAGCTGGGT ATGGTGGTGC ATGCCTGTAA TCTCAGCTAC TCCGGAGGCT 180 GAGGCGGCAG GAGAATTGCT TGAACCCGGG AGGCGGAGGT TACAGTGAGG CGAGATCATG 240 CCATTGCACT CCAGTGTGGG CAACAAGAGC AAAACTCTGT CTCAAAACAA ACAGGCCGGG 300 TGTGGTGGCT CACGCCTGTA ATCTGAGCAC TTTGGGAGGC CGAGGAGGGC GGATCACGAG 360 GTCAGGAGAT AGAGACCATC CTGGCTAACA CAGTGAAATC CCGTCTCTAC TAAAAATACA 420 AAAAAATTAG CCACGCGTGG TCGTGGGTGC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG 480 CAGGAGAATG GCATGAACCC GGGAGGCGCA GCTTGCAGTG AGCCGAGATT GCGCCACCGC 540 ACTCCAGCCT GGGCGACAGA GCGAGACTCT GTCTCAAACA AACAAACACA AACCAACCAG 600 TGGTTTTTGA AGATGACCTC ATGGGACTGT GGCCGGAGAG TCCTGATGGC CTCTGGCTGT 660 GCTCATGCCC CTGCCATAGG AGGCGGGGAC TGTCATTTCA CCGTCTCCTG ATGCCATTCC 720 AGAGGTTACG CCCTGAAGTC AGCTCAGATC CTGGGCCAGG CACTGCATGG GAGACAGGCA 780 TGAGCAGGAC CTCTTTCTGC CTTCGAGGAA AACACGGGGG CATCTGGGGC TCACTTGGCA 840 CTCATCCACC TTGTGCTGTA CCTGGGGACC TCCGGGTGGG TGGCTGTCAT AGAATTCGGC 900 TCCAAACCAG GATGCTTTTG GGAATTGAGG GAGAGCCCTG TGAGTAGCTA TTCAGGGCTA 960 TCACGGGGGC GTCGACCACC CCACTGCGTG TCAGGAGTGA CCACCAGGGT GTGTGAGTGC 1020 AAACAGGGCG GGGCCTGGGT GGCAGCTCAG CGGAGCCCTG AGCCCCCAAA GGTGGGCTCT 1080 CTCACGGGCC CTGGTCTCGT 1100
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