Tag | Content |
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EnhancerAtlas ID | HS091-02132 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr1:85599880-85601680 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:85600920-85600932 | GTTTGTTTGTTT | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I085134 | chr1 | 85599776 | 85602122 |
| Enhancer Sequence | GAGGAAAGAA AACTTTGTCG GATAGATTTT AGCTCTTAAC CACCTGTGTG CCCTTGAACA 60 GATGACCCAG CTCTGTGAAA CAGATTCCCC TTCCATCAAG TCAGGTTGAG AGAACTTAAC 120 TTGCAGCATT TATGTAAGGG GCAAATGAGC CCCTGCAGAT AAGGGGCCTG TGCCTGGCAC 180 ATATTATTGT CATCATGATT GAAATATCCC AGGGCTCATC CTTACACTTG AACTTCTTTT 240 ATTCTTTCTT TTTTCTGCAC TCACTTTCTA GGTGCATGCA TCCACTCTCA AGGCTTTAGA 300 TACTACCTCT GTCCCTGACC TGGCCTTCTC TCTAAAATCA AGAGATGTGT ATCTATTTGA 360 CCTTTTGTAT CTCCACTTGG ATGTTTAATA GGCATCTCAA ACTTAAACAT GTCCAAAATT 420 GAGTGCTTGA TGTTTCCCTT CAAAAACCAT TCCTCCAGCA GTCCTCCCAG CCATGATGCT 480 GCTTGGGGCA AAAGCCTTAA GGTCATCCTT CATCTCCTTT CTTTCACAAT CCACATCCAA 540 TCTGTCAGCA AGTCCTGTTG ACTACACGTT CAGTATGCAT GTGAAACCTG ATCGCTTCTC 600 TTCTCCCTCA CTGCTACCAC CATGGTCCAA GCTGCATCAT CATCAGCTTG GATTTTGCAG 660 CAGCCTCCTG TTCTCCCTGT TTCTATGTTG TCATTTTCAG TCACTTTCAG CCACAGCCAG 720 ATGGTAGTTT TAAATGGATG CTGTCAGATG CTGTCATCCT TCTGCCCAGA ATCCTTCCTC 780 AACCTCATAG TATGATCACT CAGAGTATGT TCCCAATGCC TGTCTGTGCC CTGCAAGCCC 840 TTGTACAGGC AGGCCTTCCA CTGTCACCTG GTCCCATCCC TCCTTCCTCT CCCCTCCATC 900 ACACCCATCC CAGTCATGCT GGCCTCCTGT TCACCAAACA TGCCAGGCAT CTTCCTCTCC 960 CTGGGCATCT GTGCTTGCTG TTCAGTACTT TCTCCAGAGA TTTTTCTAAT TTTATTTTCA 1020 CGAGTTCACT CTAAAAAATG GTTTGTTTGT TTTTAAAGAC AGGGCCTCAC TCAGTTGCAC 1080 AGGCTGGAGT GCAGTGATGC AATCATAGCT CACTGCAGCC TCAAGCTGTT GGGCTTAAGC 1140 AATCCTCTTG CCTCAGGCTC CTGAGTAGCT AGGACTACAG ACACATACCA CCACACCTGA 1200 CTTTAAAAAA ATATATTGAA TGCCTTCTAT GTGCCAGGGT CTACCATTTT AAACAGGATG 1260 GTCAGGGAAG GTGACACTTG AACAAGGCCT GAAAGAGGTG AGGGGTTTCA CCTGTAGTCT 1320 TCTAGAAGTG TGTTCCATAA CCCAGTCTCC CTCTCTTCAA TGAAAAGAAG CTGGGACTAC 1380 AGAGAACAGG TGTGTCATAA CTGAGTGTCA TAAACCATGA CTGGAGGCTG AGCACATTGT 1440 TGTCTCAAAT AAAAGCAGGG TGTTGTTAGC ATAAAGGACT GGAGTAATGG ATATTGAATA 1500 AGTGTCTGCC TTAGGGTTAG CAAATATAAA GCTTAGTATA GTGGCTAGCA TACGGCAAGC 1560 AGTAAATATG TTTTGCCTGA TTTACAAATA CAAAATGGTT GTAACATTCT TGCTATAGAA 1620 ACTAAACATG GGGCTCCTTA TGGTTATGAT AGCAGTTATT ATTAGTTCAG TGTGATTTTT 1680 GTCTTTATTC TTTTTCTTTT TTCTTTTTTT TTTTTTTTTT TGAGATAGAG TCTCACTCTG 1740 TTGCCCAGGC TGGAGTGCAG TGGCTCGTTG TTGGCTCACT GCAACCTCTA CCTCCCAGGT 1800
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