Tag | Content |
---|
EnhancerAtlas ID | HS091-01364 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr1:40074350-40076780 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:40075451-40075470 | AAGCGCCCTCTGGCGGCCG | - | 6.44 |
| | 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 |
GH01I039609 | chr1 | 40075126 | 40076200 |
| Enhancer Sequence | GGGCGACAGG GCTAAACTCC GTCTCAAAAC AAAACACAAA AAGTGTTTAG AACAGCGTAT 60 GGTCCTTAAT AAGTACTTAA ATTCAAGCTA TTATTAACTC AACCAGTATT TCTTAAGCAA 120 CTACCCTGTT CTAGTACCAC TGTTCTAGGT ACTGGGGTAG CAATCATACT CGTACAGAGC 180 TTACCTGTTG GAGCTTATAT TCTAGAAAGG GAGATGGACA ACAAAATAAG AAAAGTTTGT 240 ATTTTTTTCC CCATGAATAT GAACGAATAT GGCCAAAAAT AGAGCATGGA AGAGGACTGG 300 GAGTGCTGGT GGAGGAAGGC TTGCTACCTA AATGGGGCTG TCAGAGGCAG CTGCTCTGAG 360 GCGACATCCA GAAAAATCCA AAGGAGGTGA GGCAGCCAGC TAGGAGGCTA AGACTCATGC 420 GCATGCGTAG GAGCAGAATA TTGCGCAAAG AGGAGTGAGG ATAAGGGCTG GAGGCTGGAC 480 CACACCGGCC TTCAAGAAAG GGGAAAGGGA CCATGTGATG CTAATTTTAT GTCGTCTTGG 540 CTAGGCTGTG GTGCCCATGG TTTGGACAAA CAAGTCTAGC TGTTGCTACG AAGGCAAACT 600 TTGGAATGTG ATTAACATTT AATTAGTAGA CTTTGAGTAA AGCAGATGAC CCTCTATATG 660 GTGGGCGGGC CACTCGGTTG AAGACCTTAA GAATAATGAC TACGGTCTCC CGAGGAAGGA 720 GGATTTCTGC CTCCAGACCG CAACATCGAA ATTCGACTTG AGTTTCCAGC GTTCGCGCTT 780 GAAAATGCAA CATCAACTCT TCCTGAATTT CCAGGCTGCC AACCTGCCTG CCCTGTGGAT 840 TTCAGAGTTG CCTGTCACCT GAACATCAAA TGAGCCAGTT CCTTAAAATA AATCTCTCTT 900 CTCAGGAATG CTCTAATACT GGCCACGGTC GCAGAAGGGA GGGAAGAATG GGGCGAGGAC 960 GATGAAACAG GGCCAGCGGT GAAGTGAGGT GGGGAGCCGA TGGTGAGCCT GGAGCCACTG 1020 GGAGGGCGCC GGCCTTTGCA CTGGTTGGGA GTCCCTGGAG GGCTCAGAGC AGAAGGGAGA 1080 CTCGGTGGCC TGCAGTGTTC AAAGCGCCCT CTGGCGGCCG GGAGGAGCGG GGGCTGCAGG 1140 GACCCGGGTG ATGGGAGGGA GCCTCCGGAG GAGGCGCAGG GGCGAGGGGA CCTGGTGCGG 1200 GCTTGGACCT CGGCCGTGGC GCCCACGGTG AGACACGGAC ACTTTCTGAT GTATCCTGAA 1260 GATGGAGCGG AGAGGATGTG CGGGCACTCT GGGTGCGGGC TGTGAGAGAA GAGGTGTCAG 1320 GGTCAACTCC AGGGCTTTCG GGCTGAGTAG CTGGAAGAAC AGAGTTGCCA TTTCCCGAGA 1380 GCAGGAAGAT TTGGGGAGGA GTCTGTCCCG GAGCCGGCCG CGGGGGCAGG AGCTGGGCTT 1440 TGGACGTGTT CGTTCTGGAC GCCTCTGGGC CTTGGCTGCT GATGTCCAAG CCTGCACCCT 1500 CAGGGGCCTG GGTTGCAGAT GTGAATTTGG CGGCTCTGAG CCGGGCCTCG TCCCGACCAC 1560 ACAGGGAGGA CAGCAGAGCC TGCGCGGGAC CGGGGCCTGT GCTCCTCCCT CTGCTCCTGC 1620 AGCGCGGGCC TTGTCCTCAG AATTTCTCCC AGCCGCCCTG CGCCTCCCCA GGCGGGGTCT 1680 CCCACCAGGA GCACCGTCCT GGGGCCGAGG CAGCGGGGGT GACACTGACT CCTGCCCCCG 1740 TTCAGTGCAT GGGGCCAGGC CCTTCAGGTC AGTGACTCAC AGACAACAGG AACAAGCTTA 1800 GAAATCTTCA AACCCAGTCA CCCATTAACT GGGTCCTGAG TGAGGCCCAG CAGACAGGCC 1860 TCAGTTTCTC ACCAGAGCTG GCACCAGTTG GTCCAGGGAA GGCAAGTGGG TCTTGTCTCC 1920 TATGCCTCCC TTGATGAGTT AGGTTTAGCT TTGGGCAGGG ATGTCTTACT GTGTTCCAGA 1980 ATTGGTGGGT TCTTGGTCTT GCCGACTTCA AGAATGAAGC TGCAGACCCT CACGGCGACT 2040 GTTACAGTTT TTAAAAATAA CGTGTCCAAA GTTTATTCCT TCTGATGTTC GGACGTGTTC 2100 AGAGTTTCTT CCTTCTGGTG GGTTCGTGGT CTCCCTGGCT TCAGGAGTGA AGCTGCAGAC 2160 CTTTGCAGTG AGTGTTAAAA CTCTTAAGGC AGTGCGCCTG AAGTTGTTCG TTCCTCCCGT 2220 TCGCAGTTGT TCATCTCTCG CAGTGGGTTT GTAGTCTCGC TGGCCTCAGG AGTGAAGCTG 2280 CAGACCTTCA CCACGTTACA GTTCATAAAG GCATGCAGAC CCAAAGAGTG AGCAGCAGCA 2340 AGACTTATTG CAAAGAGCAA AAGAACAAAG CATTACACAT GCTGAAGAGA AACCCAAGCA 2400 GGCTGCCACT GCTGGCTTCG GCAGCCTGCG 2430
|
| |
|
|
|