Tag | Content |
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EnhancerAtlas ID | HS154-15552 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr3:48934220-48936120 |
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 | EWSR1-FLI1 | MA0149.1 | chr3:48934300-48934318 | CCTTCACTCCTGCCTTCC | - | 6.47 | 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 | GATTAACAGG CATGAGCCCA CCGTGACCGG CCTAGGTTGT CTTATTTTAT AATATGATCC 60 CCACTTGCAA GCCACACTCA CCTTCACTCC TGCCTTCCCA TCAGACTGTC TGGGTCTCCC 120 TACTCCTTCA GTCTGAACTC ACCCAGCACT TGAATGCCTG TTCTAACGCA CCACCTTCCA 180 TAGAGCCTTT TCATGACCCA CTCTGAAGCG CTGCAGCTTT TGCCTTGTCA GGACACACAG 240 CCCACAGCTC AGTTACACTA TCTTGGACTT CTTTTTTTTC TTCTTCTCCT TTTTTTTTTT 300 TTTTTTTAAC CTTGGAACTC TGAAAGTACC TTAAGGTCAG GCTTTGATTG GAGCCCACCC 360 AGCTCACTAA GGCCAAAAAC ACAGCAGTCA GCAATTTGTG GTTTTGGTTT AAGCTAAAAA 420 GAGGCTTTCT GGTTGCTAAA TATGCCAGTG AGCATTTCAG TTATTTGCAC TTCAGTGCAG 480 AGGTCATCCA GTCCTTCTTG GGAGTGACAT CAAGGACAAA GGTGATATGG AGGTAGGAGC 540 AATATTTGTG TGTGTGTGAA TATATATATA TATATATATA TTTTTTTTTT TTTTTTTTTT 600 AAGGGCGGCC CCAGAGGCCT AGAACTAATA AGATATCTGC CTATATGGAC CAAGAGCAGG 660 AAGAAAGGCC AGACAATCGT CCCTCAGTAG ACAGTGCCGC TTGGAATGAC CACAGTCTGG 720 GAAGCACTAA CACATGGCAT TTACCACCAG CTAAATAAAC ATTTGATTTC ATGTTGCACA 780 ATGACCTAGC CAGTCCAGCT ACTTTAACCC TGGTCTTCCT ATAGAATGAC CCCAGTATGA 840 GCTCTACTTC AGGGCAGCTC CTCTCTTGGA TGAAAGGCAG CAAAGAGCTT GCTGCCCAAG 900 CTGGCCAAGA GGAAGTGCCC ACAAAACTAT TTCGCTGTGG AAGAAATCTG ACCCAACATC 960 CTAACAAACC CCCTCACATG GGCTTCCAAT CTTTTAAAAC TCATGTCTGC TCCCCACAGG 1020 CCCACCCTGG CAATGACTTG TCAATTTCCT TCACGTCTAC GTCTAGAAAA AAAGTGAGAA 1080 AACTGGATGC AGCTTCGAGT GCTAAGCCAT GGGGGATGGA CTTTGGTCCC CAAGCAAAGC 1140 ATTAATGAAG GTGTTGCAAG GGGAATAGTT GAGATATGAT ATGAGGAAGA CCAGAGAACA 1200 ATTCCTGATG AACGTCCTCC CTCCCAAGCC TCAGTCTGAC CATAGCTTCC TCATCTGGGA 1260 GTTGTGAGAA TGAGGCTGGC CTTGTGCAAA GCTGATCACC TTGCTTTCCG TGGAAGGGGC 1320 TCGGTCACTG AGGTCATCAT TGCTTCTCAC AGGGATGCCT CTGCCCAGGA GGCTGAGCAG 1380 GCCACCGTTG GGTGACAGGC CGAAGAGTGT CAAGTATCTC CCCGGGCCGG GAAAGGTGCG 1440 AAAGAGATGG GTACTCTTGC CCCAGGGGAA TGTATCAAAG GACACCTCCA GAACAACCGT 1500 ACCGCTCTGT CTTTAGTTGT CTTCCTGGGG CAGGCTTTAC AGGGGACCTG TTTCAACCTT 1560 AACGATAATA TTAGTGTTGG CTGAAACCAA AACTATGGAG AGACGTTTAT TCCTTCCCAT 1620 CCCTAAAGAA GTGGCGCAGG GTCAGAAGAG ACTGCGGGAC AGGGAACTTT ACATCAGAGC 1680 TCTTGACAGG CAGTTAGAGG CTGCTCACTT TGCGCCGCCG CCTGGCTCTT TGGGGCGCAA 1740 GGTACAGCTT CCTGCCCACC CCTGAAAGAG AGATTCCCTA GACTTCTCAC GGAAGCTCAC 1800 ACATGCCCCT CTTCTGCCCA GCGTCCGCGC CTCGCGGGGG ACCATGCTTT CCGCGCCCCG 1860 CCCGGGCCTC CTCCCCAAAG CCTGCGACCC AGCCTCCCGC 1900
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