Tag | Content |
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EnhancerAtlas ID | HS129-13330 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr15:79217780-79220050 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr15:79218444-79218464 | GGGTTGGGGGTGGCTGGGTT | - | 6.01 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09996 | chr15:79216465-79222817 | CD14 | SE_41737 | chr15:79217303-79218120 | LNCaP | SE_41737 | chr15:79218466-79219082 | LNCaP | SE_41737 | chr15:79219088-79220303 | LNCaP |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr15 | 79217883 | 79217935 | chr15 | 79218925 | 79219947 |
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| Number: 3 | ID | Chromosome | Start | End |
GH15I078924 | chr15 | 79217304 | 79218120 | GH15I078926 | chr15 | 79218467 | 79219082 | GH15I078927 | chr15 | 79219227 | 79220602 |
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Enhancer Sequence | TACTGTGGAA ACAGGACCGA GACAGAAACA CATGGCCTGT CACCTCCCCA CTCCTTTCAC 60 AGTACAGCCT TTTGCCTCAA GCTAGGGGCT AGAGGCCCAG AGCAGCATGG ATGGCCAGAA 120 GCAGCTCCCC TGCGGCCTCT CTCCCTTCCT GTCTCTGGCT GGGTCTGTCT GGCCATCTCT 180 CGTTCCTCTC CCCAACTCTG CTCCTAGGAA ACCCTGCACC CTCTGAGATA GGGACCACGG 240 GGTACAGCGT GGACCTACTC ATTCAGTCAT TCACATCCAT TCCCTGAGGT CCTCTCCTGG 300 GCCAGCAGCT CTCACCCCTA CACCCATAAA CCCAGAGTCT ACAAAGCTTT GCTGCTAGAA 360 CACAGGGGTT ATAAACCATG GACGGGTAGG TCCCAGATGG CGGTGGAAAC GAGAAGACCC 420 ATCCGAGGGC TGTGTGACTT CTGAGTAGAA CCTGTCCCCT CCAAGGGGGA AGGTAGGTGG 480 GGGGAAGTCA GGGTGGCTTC CTGGAGGCTG CAGCTTTGGA ACAGAGCTGC AGAGACCAGG 540 TGACAGCAGC AGGTAGAACC CCATGCAGAA CCTTAAAAAA ACCCCAAGTC CAGGCTGTGC 600 CTCAGACCAA CTACAACAGT ATCTGCAGGG TGGGTCCCAG GCATTGGCAC TTTTTGGAGC 660 TTCTGGGTTG GGGGTGGCTG GGTTCAAGTG CACTAACCAA GAGACCTCTG GGAGCTGAAA 720 TGAGGGGGGA AGTTACCTGT GCTGAGGCCA GGGCCCTACT GAAGGAAAGC AAGTGCAGGA 780 GGGACGGGGC GCCCAGCCTC CCTCAGTCCT GCCTCCCTAG AGGGGTGGAC AGAGACCCAG 840 CTGTGAAAAG CAAACAGGTG CCTGGCAAGG GAGTGCCCTC CTTCCTGGTA TGTGGACAAG 900 GCCTTGTGAG CCCAACAGGT CAGGGCATAT CTGAGACATG GAGGGCACAG AGGCCAGCCC 960 AGCACAGGGG CGATGACTTC TGCAGGTGGC ACCATTTCCA CCCCATGGGC CTGCCCAAGA 1020 GGGCTGAATG CTAGTTCTGG CCTGGTCGTC AGGGCCCTGC AGGTGTCACC AATGAGGCTC 1080 TCCTGGGGAC CATGCAAAGG GATACCTTTG AGGCCCAAAT TCACCTGTCC TTGGGATATC 1140 ATGGCCCAGA GCAGCCAGCT TGAGTGACAG CAGCAACATT CTGAAGAGGG TGACATCCTG 1200 AGTACAGGAT TTGCGCTGTA TGTTGTCAAG GCAATGAGCC CTGGTTCTGG AATGACACAT 1260 TCTTAGTTCA AATCCAGCAT CTATTTCCTA GCTCTGTGGC CTTGGGCACA TTACTTAACC 1320 ACTTGGAGCC CCCGTTTCCT CACCTGTCAA ATGAGGTAAT AAGGATACTC ATCTCCTAGG 1380 GCCAGTTCGG GTCTAGAGGG GATAGTGCGT ATTGAGGGTT GGTACAGCAC CTAGAAGTAC 1440 TCCATCAAGT TAAGATGTTA TTGCTGAGAG CTTGGCACAT GCTTCAACTA AATGGCAGCC 1500 GCTGTCATTA CACAGACATC ACGTTTGTGA ACTGTACATA CATTCGTGGG CGCACACACA 1560 ACCTAAGCGA TATTCCTCCA CTCCTCACAC ACCCTCCCAC ACTTGCATGC ATGCACACTG 1620 CAGTCACGAA GGCGTTCATT CACGTTCCAG TTCTCTCTGG GAGAAGCAGG GTAAGACCAC 1680 ACTTCCCTAT TCACTTGAGG TCAACTGTGA CTGGGCGGCT TGTTTTGGCT TTAGAGCTAG 1740 GGCATCATTT ACCACCTTCT TTCCCTCTAG TCCTGGCGTG AGGCCAATGA CACGGAGCAC 1800 ACACCACCCT CCCTAAGCTG TGCATGGGCG CAGGAGTGCC ACACACCCTT TGACTGTTGT 1860 CAGCCATGCA GATTGGGCAC GGTTGTTATT GCAACAGAAC CTGGCTCATC CTGAGTGACA 1920 CACACTCACC CTCCTCAGTT TCACACACGC TGTGTCAAGC ACGTGCTCAT ACCCTCTTCT 1980 GCAGGATGCG GACAATTGCT TGCATTTTAC AAGCAAGAAA ACAGAACCAA AAGAATGAAG 2040 GCATGTGTGG ATCTGGAGTT CAGAACCAGA GGGCCTGCCT GCCAGTTTGC GCTCTCCCTC 2100 CCATCTCCTG CCTCGCCACC ATCACAGCGA CTGAGACCCA GGGATAATAT GAACTCGTCA 2160 AAGGGATGTG CTGCCAGAAG GGCTGCCTTG CTGGGCCCAC TGGCTATCCG ACAGCATGAG 2220 AGAGGCCTCC TCATCAGGAC ACATTCCCCA TCCCAGAGGG GGATCGGCAC 2270
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