Tag | Content |
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EnhancerAtlas ID | HS187-17112 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:48934370-48936120 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DMRT3 | MA0610.1 | chr3:48935688-48935699 | AATGTATCAAA | + | 6.02 | HINFP | MA0131.2 | chr3:48936038-48936050 | CAGCGTCCGCGC | + | 6.22 | HNF4G | MA0484.1 | chr3:48935336-48935351 | TGGACTTTGGTCCCC | - | 6.39 | Mafb | MA0117.2 | chr3:48934605-48934617 | AGTCAGCAATTT | - | 6.92 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr3 | 48935999 | 48936096 | chr3 | 48934891 | 48935000 | chr3 | 48935000 | 48935200 | chr3 | 48934400 | 48934409 | chr3 | 48934539 | 48934759 |
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Enhancer Sequence | TGAATGCCTG TTCTAACGCA CCACCTTCCA TAGAGCCTTT TCATGACCCA CTCTGAAGCG 60 CTGCAGCTTT TGCCTTGTCA GGACACACAG CCCACAGCTC AGTTACACTA TCTTGGACTT 120 CTTTTTTTTC TTCTTCTCCT TTTTTTTTTT TTTTTTTAAC CTTGGAACTC TGAAAGTACC 180 TTAAGGTCAG GCTTTGATTG GAGCCCACCC AGCTCACTAA GGCCAAAAAC ACAGCAGTCA 240 GCAATTTGTG GTTTTGGTTT AAGCTAAAAA GAGGCTTTCT GGTTGCTAAA TATGCCAGTG 300 AGCATTTCAG TTATTTGCAC TTCAGTGCAG AGGTCATCCA GTCCTTCTTG GGAGTGACAT 360 CAAGGACAAA GGTGATATGG AGGTAGGAGC AATATTTGTG TGTGTGTGAA TATATATATA 420 TATATATATA TTTTTTTTTT TTTTTTTTTT AAGGGCGGCC CCAGAGGCCT AGAACTAATA 480 AGATATCTGC CTATATGGAC CAAGAGCAGG AAGAAAGGCC AGACAATCGT CCCTCAGTAG 540 ACAGTGCCGC TTGGAATGAC CACAGTCTGG GAAGCACTAA CACATGGCAT TTACCACCAG 600 CTAAATAAAC ATTTGATTTC ATGTTGCACA ATGACCTAGC CAGTCCAGCT ACTTTAACCC 660 TGGTCTTCCT ATAGAATGAC CCCAGTATGA GCTCTACTTC AGGGCAGCTC CTCTCTTGGA 720 TGAAAGGCAG CAAAGAGCTT GCTGCCCAAG CTGGCCAAGA GGAAGTGCCC ACAAAACTAT 780 TTCGCTGTGG AAGAAATCTG ACCCAACATC CTAACAAACC CCCTCACATG GGCTTCCAAT 840 CTTTTAAAAC TCATGTCTGC TCCCCACAGG CCCACCCTGG CAATGACTTG TCAATTTCCT 900 TCACGTCTAC GTCTAGAAAA AAAGTGAGAA AACTGGATGC AGCTTCGAGT GCTAAGCCAT 960 GGGGGATGGA CTTTGGTCCC CAAGCAAAGC ATTAATGAAG GTGTTGCAAG GGGAATAGTT 1020 GAGATATGAT ATGAGGAAGA CCAGAGAACA ATTCCTGATG AACGTCCTCC CTCCCAAGCC 1080 TCAGTCTGAC CATAGCTTCC TCATCTGGGA GTTGTGAGAA TGAGGCTGGC CTTGTGCAAA 1140 GCTGATCACC TTGCTTTCCG TGGAAGGGGC TCGGTCACTG AGGTCATCAT TGCTTCTCAC 1200 AGGGATGCCT CTGCCCAGGA GGCTGAGCAG GCCACCGTTG GGTGACAGGC CGAAGAGTGT 1260 CAAGTATCTC CCCGGGCCGG GAAAGGTGCG AAAGAGATGG GTACTCTTGC CCCAGGGGAA 1320 TGTATCAAAG GACACCTCCA GAACAACCGT ACCGCTCTGT CTTTAGTTGT CTTCCTGGGG 1380 CAGGCTTTAC AGGGGACCTG TTTCAACCTT AACGATAATA TTAGTGTTGG CTGAAACCAA 1440 AACTATGGAG AGACGTTTAT TCCTTCCCAT CCCTAAAGAA GTGGCGCAGG GTCAGAAGAG 1500 ACTGCGGGAC AGGGAACTTT ACATCAGAGC TCTTGACAGG CAGTTAGAGG CTGCTCACTT 1560 TGCGCCGCCG CCTGGCTCTT TGGGGCGCAA GGTACAGCTT CCTGCCCACC CCTGAAAGAG 1620 AGATTCCCTA GACTTCTCAC GGAAGCTCAC ACATGCCCCT CTTCTGCCCA GCGTCCGCGC 1680 CTCGCGGGGG ACCATGCTTT CCGCGCCCCG CCCGGGCCTC CTCCCCAAAG CCTGCGACCC 1740 AGCCTCCCGC 1750
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