Tag | Content |
---|
EnhancerAtlas ID | HS044-10237 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr5:32504410-32507130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr5:32505338-32505359 | GGAGGAGGAAGGGTAAAGGAG | + | 6.56 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 32505356 | 32506294 | chr5 | 32506328 | 32506774 |
| | Number: 1 | ID | Chromosome | Start | End |
GH05I032503 | chr5 | 32503899 | 32509816 |
| Enhancer Sequence | ATGACAGTTC CGGGAACACC TGTATTTGGT GTAAAAATGG GTAGCATGAC AATTCTGAGA 60 AATGATCACC TTTTTCCAGG AATCTTCATG AATATTCCAC TCTTTGGTTA AGAAATCCAT 120 AAAGACAGAA ATGCTAAATC CCATCACAGC ACTCTCTTGA GTATGCATGC ACTCTTTTTT 180 TCTGGTGTGT GTACTTTCCC TTTGCAATAA ATCTCTGTAC TTTCACAATT TTCTGACTTG 240 TCGTTGAATT CATTCTCACG ATGGCATCAG GAGCCTGGAC ACCGGCTGGG GTTAAGGTCC 300 CACTGACATT TAGAGACCTT CCCTAGCCCA CCAGTATCAA TCTCTGCCCC ATTTTACCAG 360 CTTCCCTCTT GGTTTTCCTC TCTGGTGTGG AAAACCTCAG TTTAGAACTG TTTGAGCCAG 420 ATTGCTTCTT CTTCCTTTGC TATCCACCTT TTAGCTATTT TATTATTTTG CAAACTGCTG 480 GTAAAAGCTA CGGGGAGGAA GGGACTACAT CCTTGATTTG GTCATTGATT TAAAGACTGT 540 ATCTCCTTAT ACAGCTGGCA TCATCTTCTA CTTGCAGATG GAAAATACGC AGGCCCCGTG 600 AAAGACAGCA AAGAAACATC TTGCCTTCCC CGTCTCTCCC CCTTGGATTC CTGATCTCTA 660 CCTCTTACGG GGCTCTGCCT TCTCTTAACC CCTTGCCCTT TTCCTCAATT TAAATTGTCT 720 GTCCCTCAGC TTCATCCCAT TCTCTCCTGG ATAGATCCAG GGCTTTGAGC CAGGAGAGTG 780 CTGGAAAAAG AGGGCCTGCT CTCAGGGAGC CGCGGAGGGA GGGATCCAAA CATTGGACAC 840 TTCCCAGCTT CACACATTTT TAGGTTATTA TGTTAAGAAG CCTGTCTGCC TCATTTTGTT 900 ATTCTAGTCT ATTTCGCATT CAACCCCAGG AGGAGGAAGG GTAAAGGAGA AAAAAAAATC 960 CTTCCTGCCA CAAATAAAAT GTAGCAGATG TTAGCTGATG ATTACAAAAA GACAGTAAAG 1020 CAGGCCAAGA AACCATGGGA GGGAGGGGGT GGACCACAGC AGAGGGCGGG GGAGTGGGTG 1080 TTCGTGGAGC TGAATGTTCA GGGCAGATGC TCTGGAGGAT TAAATTACAC CGAGAGTGAG 1140 GCTGCTGGTG CCGTCCCTCA GCCCTGCTCT GTAGCGCTGG GAGCTATTTC AAGCCAGTGA 1200 GAAAGAGAGT CTGCACTATT TGTCTTTAGG AGGTGCTTTA TTTCCTTCCC TGTTTTGGAA 1260 AATGATACCT AGCTCTGCAT GCATGTGGGT GCCTTTTTTA ATGAAGTGCT ACTCAAGGAC 1320 TCAAAAGAAG GAACAGTGGC AGATGGGGCA TCTGTGGGTT TTGCCTCTTC TGCAGCCATT 1380 CCCCCCTCCT CTGGTAACAG CACTATGATT TGGTGGCGGG GAAGGGCTGG GGGTGCATCT 1440 TTTTCACTGT AAGTCCCTGT GGTTCAGGTG AGACTGATTC CATCCTGCCC AATGCCCCTG 1500 CTCCAAGCTG GGCACTTACG CCAGCCTAAG CCATTGATTG CCCTGGAATG TTCATGTGAC 1560 TTAAGTTAGG ATGAGGAGAG TCAGCTCCAG GACTTTTGCT GACACTGTTG TGAAAGAGGG 1620 GCTTTCTGCT GCGAATGCCA AGTGGATGGT ATGCAAGTCT GGAGCTGTTC CTGGCTTGTT 1680 CTGTGAAAAC TTACTGGAGA ATGAAGCCAA TTAGAAGAGA TGCATTTGAG CAATGAAGAA 1740 AGAAGTTTCC TGAGGACATT GAGCATCTGG ATCCAGCTGC AGCTGAAACT GATCCTACCC 1800 TAGGACTTTG CAGGTATATG TGGCTGTAAG TCTTCCCCCA CCTCTTTATT CTCACCACTT 1860 TGCATTTGGG TTTCTGTCCC TCACACCTAA TACAAGTGCC TTCAGAAAGC CCGGGAGGCT 1920 TGTCCAGGTC ACTGTGCTGG GCAGAACAAA ATGAGGGCAG CTATCTATCA TTGCCTCGAT 1980 GCTGCTCTTG CTGTGGATGA AGCCTGGAGG CTTATTTCCA GGTCATGTTT GACTCTGAGT 2040 ACACAGCTGC CTCTGAGAAA GATTGCCAGG CAGGAGTCAG CAGCCAGAAC TCAGCTCAAC 2100 AATCGTGTTC AGTTCTGTGT TATTGTACAG CAGTGCTCTC CAAGGACACC CTTGAATAGA 2160 AATGAATGCA CATAAAGGTC CAACATGCAT TCAGGAAGCC AGAGTCTCCA CTTGTGCCCA 2220 TATGCAAAGG AATCATTGTT CTCAGACCCC CTGGTAGAGA CAGCTCTCAG CTCACTGACA 2280 TGAACTGATG TGAAAATGTT CTTTAAGTGG AAAGCAGCAG GAAGCAGCTG TTAAGGAGGT 2340 GGGCACTTAG AAAGGAGAGA CCACTTTACC ATTTATCCAT TTGTCCAGCA TACATTGATT 2400 GACCGCCTTC TATTGTGTTA GGGACAGAAA TGCTAATAAA AGACAAAGTT CGTGCCCTCA 2460 GGAAGCATGC AGTTGAGTCA GGGAGTCAGC AAGAAAATCA ACTGGTAAAT AAATGTAATC 2520 ATGATAATTT AAACGGAAAT AATAGGAGAG TGCCATCTAC CCAACAGCAT AACTCTCTTC 2580 TTAGTTTGTA GAATCTGGAT TTTATTCTAA AAGGCAGGAT GCTCAGGTCC CTCCCCCAGG 2640 CTCAGGATTA ACTATGATAC ATCTAAGCCA GTGATTCCAA ATTTTGGCTT GCATGAGTCA 2700 CATGGAGGGC TTGTTAAAAC 2720
|
| |
|
|
|