Tag | Content |
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EnhancerAtlas ID | HS059-23533 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr19:44179500-44180520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr19:44179593-44179614 | TCATTGTTTCTGTTTCTCTTT | + | 6.31 | IRF1 | MA0050.2 | chr19:44179599-44179620 | TTTCTGTTTCTCTTTCTGATT | + | 6.38 | SNAI2 | MA0745.2 | chr19:44180422-44180432 | TGCACCTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr19:44179882-44179903 | AGAGGAGGAGGCAAAGAGAGG | + | 6.09 | ZNF263 | MA0528.1 | chr19:44179956-44179977 | GAGGGAGAGGGAGAGAGAAGA | + | 6.29 | ZNF263 | MA0528.1 | chr19:44179885-44179906 | GGAGGAGGCAAAGAGAGGGAG | + | 6.39 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09735 | chr19:44177241-44180521 | CD14 | SE_35133 | chr19:44178080-44180680 | HeLa | SE_54342 | chr19:44177634-44180240 | Spleen |
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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 |
GH19I043673 | chr19 | 44177519 | 44180485 |
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Enhancer Sequence | TCTCTGTATC TGTTTGTCTC TCTCTTCATG TCTTTTTATC TCTGCTTCTC CCTTTTCTCT 60 GTCTCTCCCC ATGGCTCTCT TTCTCTTTCT GTGTCATTGT TTCTGTTTCT CTTTCTGATT 120 CTTTCTCTCT GTCTCTCCCT CAAGTGACAC ACACACACAC CTGTAAGGTT CTGCTGACGT 180 GTAAAGGGAA GGGAAATGCA GGGATCAGGA CCTGGACACT CTCCAGAAAC ACGGCAGGGA 240 TGTCGGCTCC TTCCTCCTCG TGACTCACCT GGGCCTCACC CAGCTCTTGC CTGCCTGCGG 300 GATCATGGGT GAGGCCCATG GGTTTCGGGG GCTTCCCCAG CCTGTGGAGA GGAGAATTTC 360 AGGCAGAGAC AGAGAGGGTG ATAGAGGAGG AGGCAAAGAG AGGGAGAGAC AGAGAGAGAG 420 AGAGAGAGCT GGGGATAGAG ATGGAGGTGG GGAAACGAGG GAGAGGGAGA GAGAAGAGAC 480 CCACAGACAG ACTGGCTCAG GGGAAATCTG AGATGGGGGT GTGGGGGGAG TGAGAGAGAC 540 AGAAAACAGC AACCGAAGAA CAAGGACAGG GAGAAAGAAA AATGGGCAAG CAGGGAGAGA 600 GAGAAGATAA GAGACTGACA GAGGAGTTAG AGAAAACAAC ACACAGTTGC CTTCAGAGAA 660 CACAAAATAG ACACAGAGAT ACAGGGACAC TGTGTGTGTG CGTGTGTGCA TGTGTGCGCG 720 TGTGTGCATG CGTGTGCATG TGTGTGAGTG TACGTGCATG CGTGTGTGCG CACACATGTG 780 TTTGTGTGCA TGTGTGTGCA TGTGTGTGTG CGCGCACGTG TTTGTGTGCC TGTGTGTGTG 840 TGTGTGCATA TGTGCATGTG TGAGTGTGTG TATGCATGCA TGTGTGTGAG TGTGCCTGCA 900 TGCATGCGTG TGTGTGTGTG TGTGCACCTG TTTGGGGCTC CCTCATCCTC TTGCCACCTG 960 CCATGATGAA GTGACTGCCC TCTGGCCTGG CCGCTGGGAA GGTCCTTCTC TGGTTGGGGA 1020
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