Tag | Content |
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EnhancerAtlas ID | HS187-00672 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr1:40192730-40193940 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr1:40193006-40193020 | ATGAGTCACATCTT | - | 6.14 | PHOX2A | MA0713.1 | chr1:40193302-40193313 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr1:40193302-40193313 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr1:40193302-40193313 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr1:40193302-40193313 | TAATTAAATTA | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGGTCTGCT GCTGAGTTCA TTTTGTGAAT TTTTCATTTG TTATTGTACT TTTTGATTCT 60 AGAATTTCCA TTTAATTCTT GTTTATAGCT TCTAGTTCTT TATTGAGATT TACTATTTGT 120 TGAGTCTTTG ACATTAATTT TTTTATTTCT CTAAACATAG TTACTATAAA TTTTGTAACA 180 TATTTATAAT AGCTGTTTTG ATGTCTTTGT TTGCTGAATG CAACACCTGG TCTTGAAAAG 240 TGACAATTTT CTATTGACGG GTTTTTTTTT CTGAGTATGA GTCACATCTT CCTGTTTCTT 300 TGCATGTCTC ATTATTTTTG TCGAAAACTG GATTTTAAAA TAATATGCTG TAGTGACTCT 360 GGATTCTGAT TTTTCCCCTG AGGGTTGTTT TTATTGCAGG TCAGTTTTTT GTTTCGTTTT 420 GAGACAGGGT CTCCTCTGTC AGCCAGGCTA GAGTGCATTG GCAGAATCAC TATTCACTGC 480 AGCCTTCAGC CCCCACCCCC AGGCCTCAAA CAATCCTCCC ACCTCAGCCT CCTGAAAACC 540 TGGGACTATA GGTGCATGCC ACCATGCCTG ACTAATTAAA TTATTTTTTT GTAAAGATGG 600 GGTCCCACTG AAACGGAAAA AGTTCCCTTG TCCTCCTTCA CAGGGCGTGG GATGGGGGTG 660 TGGCTCACTT CTTCAATGCC CCGCTGTTTA AACCTCTAGG GGAGCATACA GACGGGGAGG 720 CTGCAGGGAT CCGACCCCAC AGCAGTGTCT AGGGGTGAAT GTTTACAGCT GAAGCCCCAG 780 TGGGCTTGTG TTACAGGGTG CTCTTTTAGT TTGCCGTCTA GAGGTGGCAT GTGTTAACCA 840 GCTCAATTAG ACCCTCTACC TTGTCGAAAG GACAGAGGGC TTTCCGTATC CTGGGGTTCT 900 TGCCTTGGTG TACCGGAAGA ATCTGATCAC ACGTGGGCTT GGAGAATGAG TGCAAGGTTT 960 TATTGAGTGG AACTAGCTCT CAGCAGATGG GGAACCCAGA AGAGAGATGG TTTCCCGCCG 1020 GAGTCGGGCA CTCAGAGAAC CACACTCTGC ATTGTTCTGC CAGTCGGTGG ACTGTGGGCA 1080 TACCAGTTCC TGTCGGTGCA GTGCTCTTGA CATCCAGCCA CCCGTGTGTT CCTCCGCTGT 1140 TGTGCGCTTC TCTACCTTCA GCAGCCTCTG TGTTCTTCCA CCGATCTGCT CCGCTCCATA 1200 TCCAGCAGCT 1210
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