Tag | Content |
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EnhancerAtlas ID | HS044-02828 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:121799350-121801740 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr11:121800011-121800032 | GGGGAAGGGGAGGGGAGGAGG | + | 6.07 | ZNF263 | MA0528.1 | chr11:121800591-121800612 | GAAGGAGGGGAAGGCGGGGTG | + | 6.19 | ZNF263 | MA0528.1 | chr11:121800010-121800031 | GGGGGAAGGGGAGGGGAGGAG | + | 6.52 | ZNF263 | MA0528.1 | chr11:121799746-121799767 | GGGGGATGGGGAGGATGAGAA | + | 6.84 | ZNF263 | MA0528.1 | chr11:121799738-121799759 | GGAGGAGAGGGGGATGGGGAG | + | 6.92 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I121928 | chr11 | 121799358 | 121801624 |
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Enhancer Sequence | AAAAATCAAT GTGCTTAAAA AAATAAAAAC AGAAAATGCC AGCTGCCTTT GCAAACAAGG 60 ACACTGGGAA ACAAATATAA TTGTGTTTTT TCCTTCTACA TCCGTCCGGG AACTTCGACT 120 GCTACTATGC TACATCAGGT ATGCAATGAA AGACAAACAA CGAGGACTCC AAACAGAAGA 180 GGGGAGCTTC AGTAACTGTA GTTTTTATGT TAGGGAGAGA CTGAGAGAGA AAGGAGCATT 240 GTATCTCGGA TTAACAGAAC TGCAGGATTT CATTAATGAC AGCCCAGCTT TTTAGCAAAA 300 GGAAGATAGT TAGGGCAGTA AAAGAGAACA TGACTAGAAT GTGCTCTGCT AATTGGAAAT 360 GTATATTATC TTCAGACGAT GTGAGTGTGG AGGAGAGGGG GATGGGGAGG ATGAGAAGAG 420 ACACATACTG AGAGGCCTGC AGGAGAAAAC TGGACCCAGG ACGCCCCAGA TTTGGCCACA 480 CCAGCAGGGC AGTTAAAGGG TCCTTTCTTG CTGGTAGGAA CGTCTAGTGC CAGGACCCCA 540 CCCTCCCCCA CTCCCTTTTA ATTCAATGGC TACGTAGGGG CTTCTTTGAT GGAGGCTTTG 600 AAGTCGGTGG CTTTGAGATT ACTCTTCCTC TGTGACCTTG ACCACCAGCC ATGAGGTTAG 660 GGGGGAAGGG GAGGGGAGGA GGAAGGCGCT GGAGTTGGAA AAAGGAAAGG AAAGAGAGGG 720 GAGGGGAAGG AAGGCCGCCC TAAGACATTT CTGCAGCATT CCACGACTTT TCTGATCACT 780 CTGCAAAGTT GAAATATGAT TGCAGCCTTT GCACCGGGAA GGAAAGAAAC CATTTAAATG 840 AAAAATTAGC TGCCTTAGCA GGTCAAGCAC ATAGTTACAT TAATGTCGTG TAGAACAATA 900 AATCAACTTC GATCTCCAAT TGAAAAAATG CTAATTTAGC TCAGCGATTC ACTGATTGTA 960 CTTTCCTCTG ATAGAAATCT TTTCTTTTAT TTAATGCGAA GCCGTGATTT GACAGCCTCC 1020 TCTAATGGTG CTTGCAGACT CTCAGCATTT CAGTGGAATT CTGATCATGG TTTTAATATT 1080 CCGTGCAGCT CTGCCCCCTC TGATTTCACG CTCACACATT AACGAGAGCT GACACTGGAG 1140 ATTAGACGCA GACAGCTGGA ATGCCAGGTC TTTGTTGCAG CATGGACAGG AGCCAACGTC 1200 GTTCAACCAC AGCCAAGAGG GACCTGGGAA AGTCTTCTTA AGAAGGAGGG GAAGGCGGGG 1260 TGGGGGGCTT GAGGGAGGGT GGGAGCGGGG GATGGGAGCA AAAAGAAAGG CAAGGTAGTT 1320 TCTGAAGGGC ATATGAAAAT AGATGTTTTC AGAAAGCCCT TTCGTCTCTG AAATTCACAT 1380 TGGAATCAAT TCTGGTTTAT TTAGAGGAAG TGGTTCATTA CAGGGAAATC CCAAATTGGT 1440 TGCAGTATTT TTCTGTAAAC TCTGAAAATA CAAGTGTGAT GCACGAAAAT GGAAATGGCT 1500 CCTGCTTCAG CTGCTCACTA GTTCGTCTGA GAAACAATGG TGATTACGAG CTGGAGGAAG 1560 AGTGCTTACA TAAGGAAATG TGTTCTCCCC TTTGCCTTAA AAAAAATCAC TTAGTTCCAG 1620 GTGAATAGAT GGGGAAATAA AACGAGATTT ATGAGCCAGG GCTGCCTGTG CGACTAGCGA 1680 CTACCTCGGC AAGAAAGGAA GTCGCGTAGC CTAACTGCCT TGATCCTCAT AAATTGTTTC 1740 CTGATACCAG AAATCAAATA AAGATCCATA GTTTCATCTA AACCATAAAG CCACTTGGGC 1800 TCAGCTAGTG CCGATATTGC AAAGGGGAAG GAAGGGTGCT GCCTGAGACA CTGGCTCAAC 1860 TTTGTCCGAA AGAAGATGAC AGATGACCAA AGTTGCGGAG GCGGCGCATT AATACTATGT 1920 CAAAAAAAAT TGTTTCTGCT CCTGGGGGAA ACCAATTGAG TAGAAATAAC AAATGTCCTT 1980 CTTGCTAACT GTATCATTAA TAATAATCGT ACTTTGCATT TTTATGGGAT ACCAGGATTC 2040 TAGAGCGCTT TATAAATATT CATAGGGGAA GGCTGGGGAA GGGAGGTGAA TGTACCCATT 2100 CCTGATGCCT GGCTGGAGTG ACTAAGACTC AGGGCCCTGC AGGGGCTTAA CTGGAGTGAA 2160 ACAGCAAATC ACAAAGCCCC ATGCTGCAGC TGGCTTGGAG ACATCCAGGT TTGGTCTCTG 2220 ATGCCCACTG CTCTCTCCTA TGAACAGGAA CGTGGCTGTA GTTTAGGAAT TAGATGAGCT 2280 GAACCCTCTT GTATCACTTT TGCTTGTTGT TCTTATTTGC CTTGGTGGGA CCACTGTCAC 2340 TGATATAAGT TTATTCATTC TACTAGCATA TAATATATAT AGTAATATAT 2390
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