Tag | Content |
---|
EnhancerAtlas ID | HS091-41642 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr6:80372180-80374720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr6:80373812-80373822 | GGAAATCCCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACTATTGGCC CCCACTCTCA TCCGACTTGT AAGGTTTCTG CTGAGAGATC CACTGTTAGT 60 CTGATGGGCT TCCCTTTGCA GGTAACCCGA CCTTTCTCTC TGGCCGCCCT TAACATTTTT 120 TTCCTTCATT TCAACCTTGG TGAATCTGAC AATTAGTTGT CTTGGAGTTG CTCTTCTCGG 180 GAGTATCTTT GTTGTGTTCT CTGTGTTTCC TGAATTTGAA TGTTGGCTTG CCTTGCTAGG 240 TTGGGGAAGT TCTCCTGGAT AATATCCTGA AGGGTGTTTT CCAACTTGGT TCCATTCTCC 300 CCATCACTTT CAGGTACACC AATCAAACGT AGATTTGGTC TTTTCACATA GTCCCATATT 360 TCTTGGAGGC TTTGTTCATT TCTTTCTACT CTTTTTTGTC TAAACTTGTC TTCTTACTTT 420 ATTTTGTTAA TTTTATCTTC AATCACTGAT ATCCTTTCTT CCACTTGATC AAATCGGCTG 480 TTGAAGCTTA TGCATGTGCT ACGAAGTTCT CGTGCCATGG TTTTCAGCTC CAGCAGGTCA 540 TTTAAGGTCT TCTCTACACT GCTTATTCTA GTTAGCCATT TGTCTAACCT TTTTTCAAGG 600 TTTTTAGCTT CCTTGCGAAG GGTTAGAAGA TGCTTCTTCA GCTCAGAGAA GTTTGTTATT 660 ACCGACATTC TGAAGCCTAC TTCTGTCTAC TCGTCAAAGT CATTCTTTGT CCAGCTTTGT 720 TCCATTGCTG GCGAGGGACT GCCATCCTTT GGAGAAGAGG TGCTCTGGTT TTTAGAATTT 780 TCAGCTTTTC TGCTCTGGTT TCTCCCCATC TTTGTGGTTC TATCTACCTT TGGTCTTTGA 840 TGTTGGTGAC CTACAAATGG TGTTTTTGTG TGGATGTCCT TTTTGTTGAT GTTGATGTTA 900 CTTCTTTCTG TTTGTTGGTT TTCCTTCTGA CAGTCAGTTT CCTCAGCTGC AGGTCTGTTG 960 GAGTTTGCTG GAGGTCCACT CCAGACCTGT TTGCCTGGGT ATCACCAGCA GAGGCTGCAG 1020 AACAGCAAAT ATTGCAGAAC AGCAAATGTT ACTCCCTGAT CCTTCCTCTG GAAGCGTCGT 1080 CCCAGAGGGG CACCCGCCTG TATGAGGTGT CAGTCGGCCC CTACTGGGAG GTGTCTCCCA 1140 GTTAGGCTAC ACAGGGATCA GGGACCCACT TGAGGAGGCA GTCTGTCCGT TCTCAGAGCT 1200 CAAACATCGT GCTTAGAGAA CCACTGCTCT CTTCAGAGCT GTCAGACAGG GACGTTTAAG 1260 TCTGCAGAAG TTTCTGCTGC CTTTTGTTCA GCTATGCCCT GCTCACAGAG GTGGAGTCTA 1320 TAGAGGCTGT AGGCCCTGCT GAGCTGTGGT GGGCTCCACC CAGTTTGAGC TTCCTGGTGG 1380 CTTTGTTTAC CTACTCAAGC CTCCCCAGTG GCGGCCGCCC CTCCCCCAGC CAGGCTGCTG 1440 CCTCGCAGGT TGATGTCAGA CTGCTGGGCT AGCAGGGAGC AAGACTACCA GGGCGTGGGG 1500 CCTGCCAAGC CAGGCATGGG AGAGAATCTC CTAGTCTGTC AGTTGCTAAG ACCTAGGAAG 1560 AGCACAGTAT TTGAGTGGGA GTGTCCTGTT TTTCCAGGTA CAGTCTGTCA TGTCTTCCCT 1620 TGGATAGGAA AGGGAAATCC CCCAACCCCT GTCCTTCCCA GGTGAGGTGA CGTCCCACCC 1680 TGCTTCAGCT CGCCCTCCGT GGGCTGCACC CACTGTCCAA CCAGTCCGAA TGAGATGAAC 1740 CAGGTACCTC AGTTGGAAAT GCAGAAATCA CCTGTCTTCT GCATCGATCA CGCTGGGATC 1800 TGCAGACTGG AGCTGTTCCT ATTCACCCAC CTTGGAACGG ACTTGTGATT GGATTTAATG 1860 TTTAGCTCTT TTTGCATGCC AGGCACTGCA CTAAGAACTT TATGAACATT ATGACATTTA 1920 AATTTCACTG CAGTTCTCTA TGCTGAATTA TTATCTGTGT TTTACAGATG AGGAAACCAA 1980 GGCTTTGGTA GAATAAGTAT CTTGGCCAAG GTGACACAGA CCCAACCCTT TTTGACTGTT 2040 CAGGACTAGA ACATTAATAA AGCCAACTGG CCCAATTGAG GTTCAGGCTG CTGCCTTTGG 2100 TGTCACTGTC ACTGTGTTCA GTCCAGCAAA GCCACATGTT CACAGACCAA CCAGTGTCCC 2160 ACACAGACCT CAGTGTCCCA CTTGCAGCAG CCAGAACTAC TTCCCATTCA TCAGTCATAT 2220 AAAGGTTTTT GTTAACAGTT TGATAGTTGA AATCATGTTA TGTTCCATGA TGTCAATTAG 2280 CTATTCCAGG AAACCAATGG AAAGACGGAA AGATGTTACA TTAAAACAAT TCACTGAAAT 2340 ATTTCATTTG AAAGACTTTA GGAGACAAGA TTTAGAAAAA TCTGTGTAAA GTCCCTGTGT 2400 TTTAGTACTG CTAGGTAGCC TACTACTAAT AACCATTTGT TATCATTGAA AAAGTTGCCC 2460 AGGCATGGTG GCTCACGTCT GTAATCCCAG CACTTTGGGA GGCTGAGGAG GGCAGATCAT 2520 GAGGTCAGGA GTTTGAGACC 2540
|
| |
|
|
|