Tag | Content |
---|
EnhancerAtlas ID | HS044-13099 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr8:142455000-142457450 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr8:142455196-142455207 | GGCCAATCAGA | + | 6.02 |
| | 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 |
GH08I141446 | chr8 | 142456289 | 142457403 |
| Enhancer Sequence | CCCTGGCTCC GTGGTGGTGC TGGGTGGCAT GGCTGCTGGT TTGGCAACCG GAGCCTGGGC 60 CCCTTCGCGG TGGTCGAAGA GGCCTGGGCC CATGCCGCTC CCTGGAGGGC GTGGGAGCCA 120 GGCCTGGCCA GTCAGAGCCG CACAGGCCCC TGTGGCCAAG GTGATTGGTT CAGGATTGGG 180 TATGTGAGCA AAGCTAGGCC AATCAGAGCC CAGGACTGTG CCCGTGGTGA GAGTTTTTTC 240 TCTTGGGGCT GCGGGAGCTG CCGGGGCCAC CTCCAGGGCT CCAGGAGAAC CTGCCCGGAG 300 CGGCCTGAGC AGAAACCACC CGTGGCCCCG CGCGAGGCAG AAGTCCCTGC TATATGGGGA 360 GCCTGAGAGA GACAGACAGA CGTCCCAGCT GTATGGGGAG CCCGAGAGAG AGACACGTCC 420 TTGCCGGTGG GGGAACCCAC GAGAGACAGA TGTCTCAGCT GTATGAGGAG CCCCCAGTGA 480 GACAGACGTC CCAGCTGTAT GAGGAGCCCG AGAGAGACAG ACAGACGTCC CAGCTGTATG 540 GGGAGCCCGA GAGAGACAGA CAGACGTCCC AGCTGTATGA GGAGCCCGAG AGAGACAGAC 600 GTCCCAGCTG TATGAGGAGC CCGAGAGAGA CAGACGTCCC AGCTGTATGA GGAGCCCGAG 660 AGAGACAGAC AGACGTCCCA GCTGTATGAG GAGCCCGAAA GAGACAGACA GACGTCCCAG 720 CTGTATGAGG AGCCCGAGAG AGACAGACGT CCCAGCTGTA TGAGGAGCCC GAGAGAGACA 780 GACGTCCCAG CTGTATGAGG AGCCCGAGAG AGACAGACGT CCCAGCTGTA TGAGGAGCCC 840 GAGAGAGACA GACAGACGTC CCAGCTGTAT GAGGAGCCCG AAAGAGACAG ACAGACGTCC 900 CAGCTGTATG AGGAGCCCGA GAGAGACAGA CGTCCCAGCT GTATGGGGAG CCCGAGAGAG 960 ATAGACAGAC GTCCCAGCTG TATGGGGAGC CCAAGAGAGA TAGACAGACG TCCCAGCTGT 1020 ATGGGGAGCC CAAGAGAGAT AGACAGACGT CCCAGCTGTA TGAGGAGCCC GAGACAGACA 1080 GATGTCCCAG CTGTATGAGG GGCCTGAGAG AGACAGACGT CCTTGCTGGT GGGGGAACCC 1140 GCGAGAGACA GATGTCTCAG CCGCATGGGG AGGTCCCAGT GAGACAGACA GACATTCCCG 1200 CTGTATGGGG AGCCCCCAGT GAGACAGACA GACATTCCCG CTGTATGGGG AGCCCCCAGT 1260 GAGACAGACA GACATTCCCG CTGTATGGGG AGCCCCCAGT GAGACAGACA GACGTCCTTG 1320 CTGTATGGGG AGCCCCCAGT GAGACAGACA GACGTCCTTG CTGTATGGGG AGCCCGCGAG 1380 AGACAGACAG ATGTCTCTGG CTCTTCGGGA CCTTCCAGTC TATGGGTGAG GGCAGTAAAG 1440 CAGGTAAAAG GCGCAGATCA CAGATGGTAG CTGATGGCGG GGCTGCGGCG AGAATAAAGC 1500 AGCAGAGGGT GGGAGGCGCC GAAGGGGCTG CTATTTTGGA GGGTGGTGGG GGAGGCCTCA 1560 GTGAGGTGCG GGTGAGCAGA GCCTGCAGAG ACAGGATGGC TGGGGGAAGA ACATTCCAGC 1620 AGGGGGAGGA GCAGACGGGG TGAGGCTTTC TCCCAACCCT CCCACGTTCC GGGAGGAGAA 1680 GGTTTTATTA GCTTATTAGG AAAGATTCAT GCATTTTGCA TGGTTGAACT GAATAAAAAA 1740 GGAACTTCGT GCACATTTGA ATTCGGAGGC AAGATGAGAA GAAGTGGCAT TTTTTTTAAG 1800 TGACTTGCCT TGGGGAGAGC TGTTAAAACT GACAAATTGC GTGACGCACA TCATAATACA 1860 AACAAATGAA AAGAGTTGGC CCCAGCGGTT TTTAGACTTG CTTATTGGAT TTTTGGAAAT 1920 ATGACCTGGT GCAGAGGGAA GATGAAGGCA GGCAGCCCTA CTGAGGCCAG AATACGGTGG 1980 GCGGGGGAGC GGGCAACTGG CCGTGATGTC AGCCTGAGCA TGTGCTGAGG ACCAATGAGA 2040 TGCCCAAGAG GGCATGGAAA GGCATCTGCC CCATGGGTGA GCCCAGTTCG CCTCTGCATG 2100 GACATGCTGT GTGGCCCAGG GGAAGCCTCT GACCCTCTCT GAGCCTCAGT TGCCTCATCT 2160 GTAGAGCAGG GACAACGACA TTCATCTCGA GTCCTCGCAG GAAACCCACT GGGGTAAGAT 2220 GTGGCTCACT GCATGGGTGC TTTTGGTAAC TGCTGTCCCC TTGAGGTCGC TGTATGGCAG 2280 TGACACTAAG TATCTCTACT GCCAAGCACC GTCAGGTGAC GGGTAAGTGG GACGAACACC 2340 TGTCTGCAGG TGCTGCCCAC AGCCCCTGTG GCCCTGGCCA TGGATGGGGC TCAGGTTCAT 2400 GACTGTTGTG GGTTGAACTG TGTCCCCCCG AAAAGAGATA TATTGAAGTC 2450
|
| |
|
|
|