Tag | Content |
---|
EnhancerAtlas ID | HS091-02666 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:120159580-120161990 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr1:120161072-120161083 | ATGACCTTGAA | - | 6.62 | Esrrg | MA0643.1 | chr1:120161072-120161082 | ATGACCTTGA | - | 6.02 | FOS | MA0476.1 | chr1:120160593-120160604 | AATGAGTCACA | - | 6.62 | POU2F2 | MA0507.1 | chr1:120161879-120161892 | ATATGCAAATGTG | - | 6.64 | Pou2f3 | MA0627.1 | chr1:120161877-120161893 | TAATATGCAAATGTGC | + | 6.09 |
|
| 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 |
GH01I119618 | chr1 | 120160847 | 120161098 |
|
Enhancer Sequence | AGAAAGGGAG GCCATGCCTT CTCACTCCCT CATCACCCTG CCCCAGGAGC TGGAAATCCC 60 AGAAGACACA GTCCATATGC ACAGCAACTG CCTCTCTCCT CCTTCTAGGC TCCCAGGAGC 120 TATGACACAA GACTTTAGGA CACCCCTCAG CAGCCCCTTC TCTGCAGCAC TGGGCACAAC 180 CACCTGGTAA CCACCTTGCT TCCTAACATT CACACAAGCT CCTGAATCTT ACAAGAGCCT 240 TCATGTTTGT CCTTTGGTTT GATTTCCCCA CACCTCATAC CCGCATCTTT CCACTGCACA 300 GATGGGAGCA AGATCAAGAA TACCTATAGG GCTTGGTCTA GGCTGCAGCA ACACTCAGCA 360 GTGGCTGTGG CAGTCCAGTG AATCTCAGGC TGTGAAGTCA TGTCTGTGAT TTCTACCAAC 420 TCTATTAACT TCAACACAGA AATCGGCAGA ACTACTTCAG CTAAAACCTT GAAGTGACCC 480 TCATTTCAGA CATTCGCTAA TGCTATACTT GACAAGAGAA AAGTCTAGCC AGATCCTTTT 540 CCAGCCCCTT GACAAAGTGA ACTAGCTTTT CCAAGGTTAC ACACTGTCCC TTCCCTCACC 600 CAACAAAGCC AGCTAAAGTG GGCATTGCCT GATTTGCAGC AGTGGTGGGG ACTCTGACTT 660 ATAGTTGCAG AGTCCTTGGC AGAGAATCTG CTTAATGCTG AGCCTTTGCT GAATGTATCA 720 TCTTGCCCTA GCATAACATG TGAAGCCTTG ACATGAAGTT CCCCCCGGTC CACCTCCCAT 780 CCCTTGCAGC CCCAGGGGCC AAATCCTTAA AGTCAGACTT ATAGTTGGCA AAATAATTCG 840 CCCAAGCAGG TTGGGCAGGC AGAAAACAAA ATAGGCCTTC ACCTTCACCT TTAAATGGTG 900 TTGGAATGTG TAAGCATCTC TACCTCTCTC ATATCTGTCT CTCTAGCATT GAGCACTATG 960 CCTGGCACTT GCCCACTCAG CTGAGGGGTG AACTTCTCAG GGTCTCTGCT CTTAATGAGT 1020 CACAGCCTTG GGGCCTGGGG AAGGCCAGTC ATACACAGAT GGTATCAGAA CACCCAGGCA 1080 GAACCACTCC CTACCTCAGC CCTTGATGCT TTCAGAAAAG CATCTCAGTG GAGTGTCTTC 1140 AGTGAATAAA AAGAATGCAT GGAACTGCTT CCAGTGAATC CCTGGTCTCC AGGAACTGGC 1200 GTCTGGCAGT TCTTTACTCA GGTTGGAAAT CCTTCAAATA CGTGTGTGGG AATGCCAATT 1260 TAAACATTGC ACGTACACTG ACACCTTTTT CAACCTCCTT AAAAACACAG GGCAACATGG 1320 TATATGGAAC ACCTTGCCAC CCACCTCATT GGCTTCCAAA GCTGAGCATT CCCAGCTGCT 1380 GGAATGAGAC AGGGCGCCAG CTGGATGCAG ACAGCATTGT GAACAGTGCC CTGGATCCCA 1440 CAGGAGCAGC AAGAAACTGA AACCCATTGG AATGTGCTTT GGGTTAGCAG AGATGACCTT 1500 GAAACCAGTC TAGCAGCAGA AAACTACAAT CTACAGGGTA CTTGCAGCTG TGATAGGGAG 1560 ACAGAGGAGC AAGCACTAGG CAATTCATGC TGGAGGCTGG CCAGGTGTGC TCCTCCCCTC 1620 CCACCAGGGG CAGAGAGGAT GGAAATTATG TGATTGCCAA GGGCAGCTGA GAAAAGGAGT 1680 CATGCCTGGG GTTTTGCTTT GTTGTGAGCT GAGTTGGGGG AATAAAGATC TGAGAGGAGC 1740 GGAGGAAGGC TGACTATGAG TGGTGAAGAC GGTGAAGGCC AGCAGCAGCC TTCCACACCT 1800 ATTCCATTGT CATCTGATGG ACAGCCAAGA CAAGCACTTT TCCTGGCTCT TACTTATGAT 1860 ATTGTCTTCA CTATTTGGAG CAGTTGTGTG ACAGGAGGCC TACCAGGAGC AGACAAAGCC 1920 TGATGCACCT TGCACTGCCC TTTGCCTCCA TACCCCCCAG CGGAGGAGAG GATTTGAGCC 1980 TTATGTATTA TTATACTTAC TGTAATTCCC AAGAAAGAAT GGGGGGTCTC TAATTGGTCC 2040 TACAGAGTTC TCAACCCTGT TTGCTCATTA AAATCACCTG GGGAGTTTCT ATAAAACTAC 2100 AGGAACTTAG GCCTCACTCC AATTAATTGC TCTCTTCATT TAAAAGGCAA ACAATCCAAA 2160 AAGCTCTCCA AGGTTAAAAA AATCTGTAGC TTAAACTAAT CAAACCTCAA GAATTCCAGG 2220 TTGACCAGGT ACAGTTTTTC TAATTGGAAT GTGGGCAGAG GCCCACTCAC GGCAAATTCA 2280 GGGTGAAGTA GCACAGATAA TATGCAAATG TGCCTGTATG GGTATGACTG TATTCTAATG 2340 CAACTTTATG TACAAAAATA TGCAGGGCAG ATTTAGTAGT TTGTCAACCC TTGTTCTACA 2400 AGAACATAGC 2410
|