Tag | Content |
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EnhancerAtlas ID | HS091-31194 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:44678430-44680310 |
Target genes | Number: 27 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr20:44680217-44680238 | AAAGGAGGGGAGAGATGGGAG | + | 6.13 |
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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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Enhancer Sequence | TGAGCAGAGG CCCTGGTTGG GCTTGGGAAA AGGTCAGGAC ACTTAGGAAG ACAGTCTCTA 60 TCCTTTTGTA CTTTCCTTCC TCATCACCTT CAGGATCAAA GGAAGTGCAG GCATTTCTTT 120 TCTTTTCCTT AGAGGAAGAG CCTAAGAGCC TAGACAGTGA GTTCTTTAGA ATTCAACTCA 180 CAGCATGAAA GACCATCAGA GGCAGAAGGG CCCATTTTAT GGATAAGGAA ACTGAGGCTT 240 AGACAAGTCA GGTCATATGT CTAAGGACAG AAAATGAAGA TTCAAATTAG GACTCCTTGA 300 ACTCCTACTC TAGACTCCTT CCTGCCAAAG TATAAATCTT TCAAGGTGAT TTCCCAGCTG 360 TGGACTCTTG ATCCCTACAG TCTGGGGTTG ACAAGGTGAG TATCCACATT TGATACAGGA 420 AGAAACTGAG ACCCAGAGAG GGAAAGCTGC TTGCTGAAAG TCGGAAAGCT GCTTGCTGAA 480 AGTCAGAAAG CTGGTGGGAA GCAACATCAG GATTTGAACT CAGGCCCCTG CTCTGTGTCA 540 CCTGCTCTTG GTTCCACCCA CTAGTCCATG CTTACAGGGC AGCCTACAGA ACCAATGTGG 600 GCTGTGGTGG CCAGTGTCTG CCTTAAGCAC ACAAAGAGGT GATTGGATCC CAAGGGTAGT 660 AGAGGAAGTA GGTTCTGTCT GAGGGTCAGG CCTTTCTCCC ATCAGGGCTG TGGCTAGCAG 720 TGGAGAGAGA AAAAGAGGCC CGAAGGAGCA GAGGTGAGAT GGGGAGGGGC ACCCCGATGG 780 CTTGCGACAG TCGCTGCTTC TGCCTCACTG GGCTGTTCAC ACTGATCTGT CAGGGCCCAG 840 AGCTGGAGGC CTTGACTGGT CAGTTCCATT CAACACGCGG TGGCTGAGAA TGTGCAGTGC 900 ACCAGGCACT GGGCGAGGCA CAGGGGAGAT GGAGATGTTC AAGACCAAGT CCCAGCCCTC 960 GAGGTGCTCA CAGGCTGGTG GGGAAGGCAG AGCATACACA GAAGGCTCTC AGACCCACCG 1020 GATGTCGATA AATGCTGTTA GAGTTAATAA CATCAGGGTC GTACAATGTG TTGAGTGTTT 1080 TCAATTCCTC AGGCAGGATA CTAACTAAGC CCTATGTGCA TGATGACATG TGGTTCTCCC 1140 TATTCCTAAA CAAGGTAGCT TGTCCTGACC CCTTGGGTGG TTAGGTGACT CACCCAAGGT 1200 CACACAGCCA GGAGGTGGCA GAGATAGGAG TTGAACTTCT ATCTGTTTGA CTTAGGGGTG 1260 GTGGTTAAGA GTGTGGGGGT TGGAGTCAGA CTTCCCTGAC TTGAATCCTC ACAGTAACAT 1320 TAGCTGTGTG TCCTTAAACA AGTCTTCCTT TCTCCAAGCC TCAGTTTCCC CATCTATAAA 1380 ATGGGAGTAA TAAGACTATT TCCCTCATAG TACAGTTTAA ATGGGAGCCC TTAAAATACT 1440 TATTATGCTA CTTAGAAAGA TTGTTGAAAC AAATTGTCTG GCTGTGCAGA GAAGCCCAGT 1500 TTAATTCTGG TCTGGGTGGG GGTGGTATCT GAAGACGGCG ACATTTGAGC TGGGCCAGAC 1560 AGGGTGTCAT GTACAACTTG GCAGGGGCTT GTGTCAGGGT GATGGTGGAG AGCATGTCGG 1620 GCAGGGGGGC TGTATGAGCA GTGGGAGGGT GGCAGAAAGT GTGGTCAGAT CATGAAGAGC 1680 CTTGATTGAT CAAGAAGGAA TGGGGCACAG AGATGATGGG GAGCCATGTG CCATTCTGGA 1740 GCCAGAGACT GACGTGATCA GAGCTGAGCT TCAGGAAGAT TGGGATGAAA GGAGGGGAGA 1800 GATGGGAGGG AAGGAGGCTA CAATGGGCCC AGCCAGGGCC AGGGAGGCCT GAGGCTGGTC 1860 CTTGTCTTTT CCCCCTCCCC 1880
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