Tag | Content |
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EnhancerAtlas ID | HS091-50028 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chrX:152126780-152128240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chrX:152127312-152127328 | TTGCTTTCCAGGAATA | + | 7.3 | BCL6B | MA0731.1 | chrX:152127313-152127330 | TGCTTTCCAGGAATAGC | + | 6.43 | CTCF | MA0139.1 | chrX:152127603-152127622 | CTGCCGCCAGATGGCGCTC | + | 6.38 | REST | MA0138.2 | chrX:152127849-152127870 | TTGAGCACCATGGTCAGGGAA | + | 6.28 | Zfx | MA0146.2 | chrX:152127059-152127073 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chrX | 152127400 | 152127510 | chrX | 152127800 | 152127961 |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI152957 | chrX | 152126477 | 152128070 |
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Enhancer Sequence | AAAGGTGACA AGAGTGAGCG TAGACAGCTC TTTCTAAGGA GTTTGGCTGC TGGAAGGGGA 60 AGAGAAGCAG CTGGGGTTAG GTGGGAGGAA CTAAGTTTAG AGACGCTAAA AGTGTATGTA 120 GCAGGAGTCA CCTGATCAGG TTGAACTGCA GCAGGAACAA GGAAGTTCCA TTTTGACTAC 180 TATTAGTTGC AAATTGGACC CTTATGTCAA CTTTTTCATC TGTAAAAAAA AAGGGATGGC 240 CAGGCACGGT GGCTCACGCC TGTAATCCCA GCAGTTTGAG AGGCCGAGGC GGGCGGATTG 300 CCTGAGTTCA GGAGTTCACA ACCAGCCTGG CCAACAAGGT GAAGCCCCGT CTCTACTAAA 360 ATACAAAGAA TTAGCCACGC GTGGCAGCGG GCGCCTGTAG TCCCAGAATC TCTGGAACCC 420 GGGAGGCGGA GGTTGCAGTG AGTCGAGATC ACACCACTGC ACTCCAGCCT GGGCGACAGA 480 CCGAAACTCC GTCTCAAAAA AAAAAAAAGG GGGGCAGGGG ATGAAAATGC TATTGCTTTC 540 CAGGAATAGC TATGACTACT TCCAATAAAG AAGACAAGAA GGTTCCACAT GTGAAAACTA 600 CGCGGTCACA ACGATAAGTG GGCGGGTGCA CGCACGCGCG CTGAGATCGT GCGTGCACAG 660 GCCGGGGTGC GGCCGGCGTG AGTACGCCTG CGCGTGCCGC CATTTCCTGC AGCCGCAGAC 720 TCTGCCTGCG GTGCTCGCCG GGAAATGAGA CGATCAACAA AGAAAATGGT TGTTTTGGGC 780 GAGATCGACC GTGGAGAGGC TTTTTCTGCA GCAGTCCCGG TTCCTGCCGC CAGATGGCGC 840 TCGAGGATCA CAAATGGGTC TAGGGTTCTC ATAATGGCCC CGCCTAAGAA ATTTTGGATT 900 CTCCTGGCCC TTCCCCCCTT TGTGGGGTCA ACAGCGGATT TGGGAATCTG GTGACCAACA 960 CGTGCGCACT CCCCTACCCT TGCCCCTACC GAGCCCTCCA GGGTAGCTTG GGGGAGAAGC 1020 TCCTCCCTAG ACTGCCGGGT ATTTGATGAG CCTGGCCAGC GCACAGGTCT TGAGCACCAT 1080 GGTCAGGGAA GAAGGCTGAA TGGCTTAGGT CTTCCTAGAG AGGCCGGAGG CGGGAAAGAA 1140 CTGGAGAAAG GAGAGATGGC AGTGGGAGGA TGGGGACAAG AATACCAGTG TGTTTCCAGC 1200 CAGAAGACGA TGTCTTTTAA CACCTCATTG AAGTCGTCAG GTGACTTTGC CCTTGTCAGA 1260 AAGGAGCAGC ACTGCGGGGG TCCTACTGAG GAGGAGACTG ACTGCTCCTT GGGGTGGGGA 1320 TTGTGCCTCC TTCCTGTCTG CCCCACTCTT GGGGAGATGA GTCCCTCCAA GTCCACGAGA 1380 CATGACAGCC AGCCTACCTG CCATGGGAGA ACAAAGTCTA GTCTCAGGGC ACTCACTTCA 1440 TAAGGGTCTT ATTCTTCCTC 1460
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