Tag | Content |
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EnhancerAtlas ID | HS091-16870 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:28335170-28337250 |
Target genes | Number: 18 | Name | Ensembl ID |
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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) |
IRF1 | MA0050.2 | chr16:28337202-28337223 | TTTTTCTTTTTCTTTCTTTTC | + | 6.31 | Nr2f6(var.2) | MA0728.1 | chr16:28335323-28335338 | GAGGTCAGGAGTTCA | + | 6.22 | Zfx | MA0146.2 | chr16:28335299-28335313 | GAGGCCGAGGCGGG | - | 6.01 |
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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 |
GH16I028324 | chr16 | 28335496 | 28336650 |
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Enhancer Sequence | CCACTGGGTG GCTGTCTTTT CTCAAGTTTG GGGTGGAGAG GGCGGTGGGG GTGGGGGCAC 60 ACAGGTACTC TAGAAACTGA AAACTTGGGC TGGGCGGAGC GGCTCACATC TATAATCCCA 120 GCACTTTGGG AGGCCGAGGC GGGCGGATCA CCTGAGGTCA GGAGTTCAAG ACTAGCCTGG 180 CCAACATGGT GAAACCCCCA TCTCTACTAA AAATATAAAA TTAGCTGGGC GCGATGGCGC 240 ACGCCTGTAC TCCCAGCTAC TTGGGAGGCT GAGGCAGAAG AATCGCTTGA ACCCGGTAGG 300 TGGAGGTTGT AGTGAGCTGA GATCGCGCCA TTGTACTCCA GCCTGGACAA CAAGAGCAAA 360 GTTCCATCTC AAAAAAAAAA AGAAAACTTG ACCTTGACAT AGGCTCTAGG CCTCCTGTGA 420 CCTCTCAGAA CTTGAGCATG AGGGGAACAG GACCCAGATT CTGGGACAAG GGGTAGGCAG 480 TTGTCCCTTG CCTGGAGTTC AGCTTGTAGC CCTTCAGCCT GGCCAGAAAA GAAGCAAAAG 540 CCCAGAGGCA GACCAGTTCA CCACTCAGCA CCTTTTTACT GAGCACCTTT TGTGTACCAG 600 GATTCCTCCT AGGGGCTGGG GACACAGCAC TGAGCAGGAC AGACAGGGCC CCTGCCCTTA 660 GGCAGCTGGT GATCTAATGA TGAAGGCAGA CATTGCCCAA ACAGCAGGCT GAGCTCAGTG 720 AGAGCATGGA ACTGGGAGAC CCATCGAGTT TGGAGGAGCC CACAGACGCT CCCTGACGAT 780 GGGGCCAGAG CAGGGGACAG GAGAAAGCTG AAAGGGCCGG TTGTGGGTGT AGACTCCAGC 840 AACAGTCAAG GCGGATGTTC TGAAGGAGGG GGAGCTTCAG TGGACTGTAG GGAGTTTCAT 900 GATTCAACAC TCATTCAAAC AAATATTTGC TAATTACCTA CTCATGTCAA CAGAGCAGTT 960 CTGTTGGCTC TGCCTTCAAA TACAGGCACA TCCCAAGGCA GCAACTGCCC ATTGCCTGCA 1020 TTGCTGCCCC TGGACATGGC CTCCCTCCCT GGCCTAAGGC AGGAGCCTCT TCTGAGCCTC 1080 TGCAGGTTCT TCTTTTTTTT TTTTTTTCCC AAGAGTTGGG GTCTCGCTCT GTTGGCCAGG 1140 CTGGAGTACA ATGACATAAT CATAGCTTAC TTGCAGCCTC GATCTCCTGG GCTCAAACAG 1200 TCCTCCCACC TCAGCTTCCC AAGTAGCTAG GACTACAGGC ACATGCCATT GCTCTGGGCT 1260 ATTTTATTTT TATTGTTACT TTTTGTAGAG ACAGGGTCTC ACTATGTTGC CCAGGCTGAT 1320 CTCCAACTCC TGGACTCAAG TGATCCTCCT GCTTTGGCCT CCCAAAGTGC TAGAACTACA 1380 GGTATGAGCC ACTATGCCCG GCCAGACAGA TCCTTTTGAT AAGATCTGTC ACTATGTTCA 1440 GAACCCTACA ATGGCTTCCT ATTCCACCCA AAAATCAAAG CTGAAGTCCT TAGAGTGGTC 1500 TCCAAGGTCC CACGAGCTCT GAGAGGTCAC AAGAGGCCTA GAGCCTATGT CAAGGTCAAG 1560 TTTCAAGCCC AGCACATTCC AGCCTCATCC CTACCATCCC CTGTACTGCC TGCCAAGCAT 1620 GTGCTCACCT GGAAGCCTTA AACTTTGCCT TGTACTCTCC CAGGGATCCC TCCCGCCCTT 1680 CCTTCAGGGT CAGAGCAAAC TTCCTGAGCC GTCTAGGTGG AGAGAAGCCC TCCTTAGCCT 1740 GCTTCACTGC ACACTGAGCA CTCGTCACCA CCTGCAGGAC CATGTATTTG TTTGTTACCC 1800 ATCTCTCCCC CCTAGAATGG AAGTTCCATA AGAGCAGAGG CAGTGTTTGG CAAACTGCTA 1860 CTTCCCTCCA GCCCCCACGC CTGGGACAGG GCCTGGTACG GTGATGGGAA CTCCGTAACA 1920 ACTTGTCAGA CTAATGAATG CATGCCTGCT ACTATTTTCG GGGCCAAGGA AACAGCAATA 1980 AACAAGACAC ACAATCCCTA TCACATACCC TGAGACATAC TCTTTTTTTC CTTTTTTCTT 2040 TTTCTTTCTT TTCTTTTTTT CTTTTTTTTT TTTTTTTTTG 2080
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