Tag | Content |
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EnhancerAtlas ID | HS187-05764 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:53810970-53812300 |
Target genes | Number: 20 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr12:53811825-53811837 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr12:53811829-53811841 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr12:53811833-53811845 | GTTTGTTTGTTT | + | 6.32 | Zfx | MA0146.2 | chr12:53811758-53811772 | CCCGCCTCGGCCTC | + | 6.01 |
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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: 2 | ID | Chromosome | Start | End |
GH12I053417 | chr12 | 53810957 | 53811930 | GH12I053418 | chr12 | 53812035 | 53812108 |
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Enhancer Sequence | ATACATGGAT TATAATCCAT TACTATTTTG TTGCTCAGAT TTTCCCAGCT ACAGTCATTG 60 TTATCTTTTG TCAGCCTATA AGCATGTTCT GGCTGGGCGC GGTGTCTCAC CCCTGTAATC 120 CCAGCACTTT GGGAGGCTTA GCTGGGTGGA TCACTTGAGG TCAGGAGTTT GAGACCAGGC 180 TGGCCAACAT GGTGAAACAC TGTCTCTACT AAAAATACAA AAACGTAGCC GGGCGTGGGG 240 GCAGGTACCT GTAATCCCAG CTACTTGGGA GGCTGAGGGA AGAGAACTGC TTGAACCGGG 300 AGGCGGAGGT TGCAGTGAGC CAAGATCACG CCATTACACA TTGCCTGGGC AACGAAGCGA 360 GACTCTCAAA AAAAAAAAAA ACATGTTCAA GTATTCCCCC TTCCCCCATT TTAAAAAACC 420 TCAGCTTCCT CTTCAAGCTA CTGATTAGTT TTTTCCATTT CCAAAGTTAG TGAAAGTAGT 480 TTACACTCAT TTTTCTCTTC CTTTATTGAA TCCTCAGGCT ACTTTGTGGG TTTGCTTTTG 540 TTTGTTTTTT TTGTTTTTGT TTTTTGGGAT GGAGTCTTGC TCTGTCACTC AGGCTGGAGT 600 GCAGTGGCAC GATCTCAGCT CACTGCAACC TCCACCTCCT GGGTTCAAGC AATTCTCTTG 660 TTTCCGCCTC CCAAGTAGCT GGAATTACAG GCACGCGCCA CCATGCCCGG CTAATTTTTG 720 TATTTTTAAT AGAGACGGGG TTTCACGATG TTGGCCAGGC TGATCTTGAA CTGACCTCAG 780 CTGATCCACC CGCCTCGGCC TCCCAAAGTG CAGGGATTAC AGGCGTTAGC CACCGTGCCA 840 GGACTGGTTT TTTTTGTTTG TTTGTTTGTT TGTTTTGAGA CAAGGTCTGG CTCTATCACT 900 CAAGCTGGAG TGCAGTGGCA TCACTCTCAT CTTGCCGCAC TGCAACCTCC ATCCCCTAAG 960 CTCAAGCTGT CCTCCCACCT CAGCCTCCCA AGTAGTTGGG ACTACAGGCA CGCGCCATCA 1020 CACCCGGCTA ATTTCTGTAT TTTTTGTAGA GACAGGGTTT CGCCATGTTG CCCAGGCTGG 1080 TCTGGAACTT GTGAGCTCAA ACAATTCACC TGCCTCAGCC TCCCAAAGCG CTAGGATTAA 1140 AGGCATGAGC CACTGCGCCT AGCCCAGGCT ACTTTGTTCA GCATCCATCA TTTACCAGAA 1200 ATTTTCCTGT TAGCATCAGC CATCTGGTTG CCAGCTCTGG TGATCTTTCA ATTATTAACC 1260 TCTTAGACCT CACTGCTTCA ATGTGCTGCT TTTGACTACT GTATCTTAGA GCTTTCTTCC 1320 CATAGAATGT 1330
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