Tag | Content |
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EnhancerAtlas ID | HS187-01839 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:171753640-171755010 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Spz1 | MA0111.1 | chr1:171754106-171754117 | AGGGTAGCAGC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 171754065 | 171754212 | chr1 | 171754766 | 171754820 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I171785 | chr1 | 171754141 | 171754340 |
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Enhancer Sequence | TGAGTTGGGA TTGCTCCCTC TCTTCCCTGG AGGGGCTGGC TTACAGGGGC TGGGGCTTGG 60 GCTGGGGCTG GGGCTGAGGC TGGGCTGGGG CTTTGGTGGG ATTCTGGACT GTTTTTTGTC 120 TTGCAGGGGT TTGTACTTCC AGAGGATTAG ACTACCCAAG GCATGATGAA AGGAGAGTAA 180 TAGCTCTCTA GCAACCTACT TGGAGTTGAG ACCTATTCCT TTTCATCTGC CATTGCAAAG 240 GCTTGATGAA GTGTGAGAAT GGGGTTGGTA GGGAAGAGAG AGAATAGAGA TAAATTTAGG 300 AGGTCACATA TGATATAGAG ATGCTAGTTA CTTTGTAGCA TGGAGTAATG GAAGTAATGC 360 TGGACTAGCA AGTCTAAGAC ATAGGTTCTA GTCCCAGCTG TAGCCTGTGA GCTGCAGGAC 420 CTGGGGAAGT TGCTGTGCTT CTCTGCAAAA TTTGGAGAGG CAGCATAGGG TAGCAGCTAA 480 AAAAGTGAGC TCTGGAACCA GACTGTTTGG GTTTCAGTTT TGGCTCAGTC ATTTCCTGAT 540 GGTGTGACAT TAGACAGGTT ACTTTTCTTT CTCTGCCTTG ATGGGATTGT AACTCTGGTG 600 TAGTTGTGAG AAGTATAAAA GCTCTTAGAA ATGGTACCTG GCCTTGGAAG TGCTGTGTAA 660 ATGTTAGCCA TTATTACTGA AAGCAGTAAG TTATATCAGA TTTATCTTAA TAAGGATAAA 720 AAAGATAGTA GGAGGAAGTG CTTTCAAAAG TGGAACATTG TAGACAAATG CAAAGTGTTT 780 ATGGTCTTGG TGTTACGGTA ATTTGTTTCC TGGTGACTGA GCTAGTTTTT CAAGTATTCT 840 ATAATTCTGT CTGTCCATGT GTGGAAATAA ATAGTGCAGT GAATACAAGC GTGGGTAGAG 900 TCTGGGGCTA GACTGCCTGG GTTTGAGTCC CAGCTTCACC ATTTACTTAT TGTGCGAAGT 960 TGGGCAAATA GTGTAACTTC TGTTTCTCAG TTTCCTCATA TGTAAAAATG GGAATAATAC 1020 TACTACCTGC ATCTTGGACT GTTGGAGGAT TCCATTAATA TATATTTGTC AACAGCTTGG 1080 AGTCATGCCT GGCATGGCTT ATTTGTGTTG GCATTACTGC TGTTTTTCTT GTGGTAGGTG 1140 TCTGCCTCCT TCCCCTACGG ACATGCCCAC ACTTCTTCTC CACCCTTGGT CCTGCCTTAT 1200 GTCTGATGGG CTGCTTTGCC CTAGATGTTG TGAACTAGAG AATTGTTAGC TCCTCAGTGG 1260 GTCACAGTTG GGGAAGATGC TGGTCTTGGA CAGGGACTGG CTCCCTGCCG TTTGGGCCAT 1320 ATTGGTTGTG GGCTTGATCA CTTTCCAGGA CTCCCTGTAA CCAAGTTCTT 1370
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