Tag | Content |
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EnhancerAtlas ID | HS105-55439 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr3:48934820-48936120 |
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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 48935999 | 48936096 | chr3 | 48934891 | 48935000 | chr3 | 48935000 | 48935200 |
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Enhancer Sequence | AAGGGCGGCC CCAGAGGCCT AGAACTAATA AGATATCTGC CTATATGGAC CAAGAGCAGG 60 AAGAAAGGCC AGACAATCGT CCCTCAGTAG ACAGTGCCGC TTGGAATGAC CACAGTCTGG 120 GAAGCACTAA CACATGGCAT TTACCACCAG CTAAATAAAC ATTTGATTTC ATGTTGCACA 180 ATGACCTAGC CAGTCCAGCT ACTTTAACCC TGGTCTTCCT ATAGAATGAC CCCAGTATGA 240 GCTCTACTTC AGGGCAGCTC CTCTCTTGGA TGAAAGGCAG CAAAGAGCTT GCTGCCCAAG 300 CTGGCCAAGA GGAAGTGCCC ACAAAACTAT TTCGCTGTGG AAGAAATCTG ACCCAACATC 360 CTAACAAACC CCCTCACATG GGCTTCCAAT CTTTTAAAAC TCATGTCTGC TCCCCACAGG 420 CCCACCCTGG CAATGACTTG TCAATTTCCT TCACGTCTAC GTCTAGAAAA AAAGTGAGAA 480 AACTGGATGC AGCTTCGAGT GCTAAGCCAT GGGGGATGGA CTTTGGTCCC CAAGCAAAGC 540 ATTAATGAAG GTGTTGCAAG GGGAATAGTT GAGATATGAT ATGAGGAAGA CCAGAGAACA 600 ATTCCTGATG AACGTCCTCC CTCCCAAGCC TCAGTCTGAC CATAGCTTCC TCATCTGGGA 660 GTTGTGAGAA TGAGGCTGGC CTTGTGCAAA GCTGATCACC TTGCTTTCCG TGGAAGGGGC 720 TCGGTCACTG AGGTCATCAT TGCTTCTCAC AGGGATGCCT CTGCCCAGGA GGCTGAGCAG 780 GCCACCGTTG GGTGACAGGC CGAAGAGTGT CAAGTATCTC CCCGGGCCGG GAAAGGTGCG 840 AAAGAGATGG GTACTCTTGC CCCAGGGGAA TGTATCAAAG GACACCTCCA GAACAACCGT 900 ACCGCTCTGT CTTTAGTTGT CTTCCTGGGG CAGGCTTTAC AGGGGACCTG TTTCAACCTT 960 AACGATAATA TTAGTGTTGG CTGAAACCAA AACTATGGAG AGACGTTTAT TCCTTCCCAT 1020 CCCTAAAGAA GTGGCGCAGG GTCAGAAGAG ACTGCGGGAC AGGGAACTTT ACATCAGAGC 1080 TCTTGACAGG CAGTTAGAGG CTGCTCACTT TGCGCCGCCG CCTGGCTCTT TGGGGCGCAA 1140 GGTACAGCTT CCTGCCCACC CCTGAAAGAG AGATTCCCTA GACTTCTCAC GGAAGCTCAC 1200 ACATGCCCCT CTTCTGCCCA GCGTCCGCGC CTCGCGGGGG ACCATGCTTT CCGCGCCCCG 1260 CCCGGGCCTC CTCCCCAAAG CCTGCGACCC AGCCTCCCGC 1300
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