Tag | Content |
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EnhancerAtlas ID | HS091-39855 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:179278950-179280370 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr5:179279338-179279350 | AAGTAAACAGTA | + | 6.18 | Foxa2 | MA0047.2 | chr5:179279335-179279347 | CCTAAGTAAACA | - | 7.22 | Nr2f6(var.2) | MA0728.1 | chr5:179279064-179279079 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr5:179279696-179279717 | GAAGGAGAGGAAAGATGAGAG | + | 6.07 |
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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: 1 | ID | Chromosome | Start | End |
GH05I179852 | chr5 | 179279263 | 179280597 |
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Enhancer Sequence | TGAGTGACAG AGCGAGACTC CGTCTAAAAA AAAATAAAAA AATAAAAAAT ATCAGGTGAA 60 GGCACTCACC AACATTATGA AATGTTTTTG TCTACGGAGG CAGGTGGATC ATTTGAGGTC 120 AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAACCCCG TCTCTATTAA ACATACAAAA 180 AACAAATTAG CTGGGTGTGG TGGCATGCAT CTGTAGTCCC AGATACTCAG GAGGCTGAGG 240 CAGGAAAACT GCTTAAACCC GGGAGGCGAA GGTTGCAGTG AGCCGAGATT GCGCCACTGC 300 ACTCCAGCCT GCATGACAGA GAGAGACTCC ATGTCAAAAA AAAAAAAAAC CCCAAAAAAC 360 AGCAATTTAA CTTTTAGGAC TTTGTCCTAA GTAAACAGTA AACAGCTGGT CACGTGGATA 420 AAGAGGTTTT TGTGAAAAGC TTCACGGTAG AGTTGTGCAT AACAGTCAAA AGGGAAATCA 480 ACCTAAATGC CCAACAAGGT TGGGCCAGTT CCTTACTCAC TCCACAAACA CCGAGCACTG 540 TGCTAGGTGC TGCGGATACA CCAGCAAATA AAAAGCCTCT GTTCTCACGG AACTTACAGC 600 CTTAGATGGA CAATCCGTGC ATAAACACAT GACTATGTAA CTTCCATAGG ATACTGAGAA 660 GAGGGAGGGG AACTCCACAG TGAGCACAAA GGCCTGAAGA GGGAGCAAAT TTGGGTTTAA 720 GGTCAGAAAG AAAGCACATG GCTGTAGAAG GAGAGGAAAG ATGAGAGGTG AAGGGAGAGG 780 TGGCACTGGG GCTGGAGCAG GAAAAGAGCA AGTTCAGTAA GGCAAAGGAT GCAGGACAGT 840 TTGGGGTCCT AGAGTTCAGG AGGGGCAATA CGGATGGACT GAAAAGACGT ACTGAATGCC 900 AGCTGCAAAC AGCTGGATGA GAGCATTTAC AGCCTGCCCC TGCCTGCCTC CACTTCCTGA 960 GCCCACTATC CCACACCTCC ACCTCCACCA ACGGCCTCTG CCCTTCCCCG GCTGCCCTGA 1020 TTCCTCTGTC ATCTTCTCAC AGTCCCCAGT GCTTTCCTTT CCTTGTGCTC AGCCGAGTTT 1080 TAAATTATGC AGATGCATGT GTGCATTAGT TTCTCTTCCC CTTCCACACA AGTGCATCTG 1140 TGAGGGCAAG AATGACAATG GGCTTACTTT CCACTGTTCC CCTTGTGCTT GGCACACAGA 1200 AAGTACTCAA GAAATACTTG CTGAATGAAG AATCAAATGG CAGTACCTTT CCAGATTCTG 1260 CTCCATCCAT TTCACTTCCT GAAGGAACAG GAAGCTCGGA AGCAGGAGCT CCGTGTCTGG 1320 GGAACTCTGT TTGAGAGAGG ATGATCCCAG CTGTGGCATG CTGGGACTCC CTGGAAGGGC 1380 TCGCTGCAGG CCTGCGCCCC ACTTGCTTTC TGTTTTGTAG 1420
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