Tag | Content |
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EnhancerAtlas ID | HS127-11332 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr16:277430-279270 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr16:278770-278781 | TACTTGGCAGA | + | 6.62 | NRF1 | MA0506.1 | chr16:279172-279183 | CGCGCAGGCGC | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATCATTTCTG TGTTCTCCCC ATCAAATGCA ATGAAAAGCT GATCTAAAGA TATTTACAAC 60 TGGAGTGGAA TACACATTTT TTTGAGGCTA GTTATATCAT GGAGAATCAC ACTTAATGAG 120 ATCTGACTCC ATCACTGTAC CAAAGAAGTC AAGGAGTCAG ACGTAAACAG CTGAGCACCA 180 AAAGGCCATT GGCTCCACAT ATACATGTGG CAATGAGACT GCAAAACCCA AGCTAATCAG 240 AGGTCCATGA ACCACCAAGG GTGACTTATA GAGCTGGTAA TTTCCACCAA CAAAAGCTAC 300 TTATTAATCT AATCTTTTTG TTATGAACAA ATGCAGAGGC AGTATTTTGC CCAAAATTGA 360 ATGAAGAAGA AAGCTTTCAA ACTCTATCGA AGACTGTTAA ATAATCTAGA TCTATTCTTC 420 CTACGTCCCT TTCGTTCCCA CCCTTAAAAA AGAGAGTTGC TACCTGGGAG TCACTTTTAA 480 CAAGACAATA CCAAAAAAAG CAAAAAAGGA ACTAGGTTAG TCAATACACA CTGTGAGCTC 540 CAACACATAC TGTACCCATC TGCATTCTTC AAGACCTCAG CTGCAGAATT TTATGCCCGC 600 TGTTGAAAAG TGTTAAAGGA AAAGTTTTCT TGCCCACACC TGCAGTAAGG AAGTCGGGGG 660 AATGATACAT AAAAGTAAAG GTAAAGTGGT ATGTGACAAA TTTTAAAGCT AGTCTGTGTA 720 TACAACACAG AGCTGTGCAA CGCTAGAGGA GGAATATATT TTAGGATTTG CAAGCATCCA 780 GGATTAATGT AGTGTCTTTT TATTGAAAAT GTTTTCTTTC TAAACTACAC TTTTAAAGTT 840 ACTTGTGAAA AAAAGCAAAC ACTTTTTTGT TATAACAGCT TAGAAATTGG TTGTGACTCA 900 CGGCTCGATG AACATGAGGC TTTCTGCAAC TCCCTTGCAG ATTGATGTAG GCAGGCAAAG 960 ATACACTGAA CCTTTATAAA TAAAATAGAG GGGCCACAAT TGTTCAGTTT GTATGAAATA 1020 AAAATATGGG AAGCAATTCA AAAGCAACTC AATATACAAA GAAAGCTAAA AAGCACTTAT 1080 TCACCTATGA AATAAAGTGC AAATAATCTG CACAGCCCTG AGAATGTGCC AGTGTGAACT 1140 TACAACTTCA TTACTCAGCA GAAAAGAAAA CACAAACCAC AGCAGGTATA TAGTTTTGCA 1200 AAGATGCAAC CGCTTTCTCC TGTGACAACC ATCATGATCT TGAGCTCCTC CCTACACAGT 1260 ACAACCTACC TAACGACTGT CAAGCGCTGG CTACACAGAG GCTCTCCTGT GTGCTGGGGG 1320 GAAGGGGGCA GCTGGAAAAG TACTTGGCAG AAACCCACGT TAGAAAAGCT CAGTTTACGG 1380 TTCCCCTTGC AATGGTACAG AACCAGAGCG GGCCAGGTTT TCGAGGCCCA TCCGGCTCCC 1440 TCGGGTGTAG CTTCTTCCCA AGGAGCCTCG GAAGAGTTCT GCCACCCGGC TGCCAGCGAC 1500 CTGGAGCCCA CGCTGATTCC AGCCCTCCGC CGACTCCACA GTTCGCGGAG GGGCACGGAG 1560 CCGCGGCGCC CGCCGGGGAG GAAGTAGCAG GACGGTACAT AGGAAGGAGG CTGAAGCCCC 1620 ATCCATGGCG CAGACTCCGA GAGAGGAGCC CGACCTGGAC CCACGGCCGC CTCAGAGACG 1680 CACCGGCTTA GACAAAGGCC CGGCGCCTGC GGTCGGAGCG CGGGGGAGGA GGAGCGATGC 1740 CCCGCGCAGG CGCAGGCGCA GACGATCGCG GCCCCCGCCT CAGGCCGCCC GGCGGCCTCG 1800 CCTCACTCCC ACCCCAGACC CTCGCCTGGT TGGCCGCTCT 1840
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