Tag | Content |
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EnhancerAtlas ID | HS092-01630 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:54041390-54042790 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr1:54041569-54041583 | GGGCCCCAAGGGGG | + | 6.44 | ZNF263 | MA0528.1 | chr1:54041909-54041930 | ATCCTCTCTCCTCCATCCTCC | - | 6.01 | ZNF263 | MA0528.1 | chr1:54041912-54041933 | CTCTCTCCTCCATCCTCCTCA | - | 6.61 | ZNF263 | MA0528.1 | chr1:54042711-54042732 | TTTCCCTGTTCTTCCTCCCTC | - | 6.6 |
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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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Enhancer Sequence | GGATTGAGTG AATGAATGAA CACACACAAA CAGTGACACC CATGCAGGAG CAGCACTGGG 60 CTGGGATGGG TGCAGGAGGG GCTACACAGG AGGATTCTGT AATGCCCTCT GATTATGCCG 120 CCCTGCGGGT CCCCTCTGTA AGACACAGGG CACATGCACA GTCAGGAGGA GATCAAAGAG 180 GGCCCCAAGG GGGTACAGTG GGCACGAACA ACCAAAACCA CTCTGCTCTT GTGTGTCCCC 240 AGGGAAAGGA CAGTCAAAGT CATCACTCCA CACCGTGCTT GCTGCACCCC AGGGCTTAGC 300 AAAACACCCT CAGAGGAGAC AGACTTGCTT TCTCTGCCTC CTCACCTCAG ATGCCCACCG 360 CCCCTTTCCT ACCCGTCCCC CTCACCAGCT CCTGGAGACG TGTACCCCGG GTACTTCACA 420 CTCCACACTC AGCAAAGGCC CTGTTTCTGA GGCCAGGCTT CCTCCCTGAT CCAGGCCCAG 480 CCACATTGGG TGACTTCCTA TCCTGGTCTC CTTCCCCAAA TCCTCTCTCC TCCATCCTCC 540 TCAATGCCCC CTCCCAGATC CACACATCCT ACTGGGGCAT CAGATGCAGG GACAATCTCA 600 GCTCCAGCAC TAGCTGTGTG ACCAAGCATA CGTGACTTAA CTTTGCTGTG TCCCATTTCC 660 TCATCCATAA AAGAGAGAGA ATAATACCTA TTTTGCAGTG TGAGATGACC CATGTAAAAC 720 CCTCAAGCAA TTCCTGGCAG ATGGCCATGG TGATCACTGA GCACAGCTGC CTCTTCTTCC 780 AGCTAGTTAG CTAGTGCACC CCTGACCTCC CGCCTCCCCA TCCACTGGGC CTCTCTGGCC 840 CCCACCTCCT CACTGCCCAG CTCAGATGCC TCTCCCTGTC CTTCTGGCCC TCTCAGCTGC 900 TAGGCTGGTA TAAACCCTGA GCAAAATGCA TGGATCAGCT CCGCCTTCCT GGATTCCAGC 960 TGCTAAGAAG GCAATGACCA CAACGTGCAC ACACATATGC ACACATACTC GTGCATGCAT 1020 GCACAAACAC ACACGCCTGC ATACAGTCCA CACCAGCACA GGCTCGAGGG CTCAACTCTG 1080 TACCCCACTC TCCTCAACCT AAGCCACCTG GTCTGCTGTG CAGTCAGTTT TCCCTCAAAT 1140 GTCCCCCTCG GCTGCTTTCA AACTGCCCTT TTCTCCTCCA GCCCTTCTCA TTCACATTCT 1200 AACAAGGCCC AGGTTCCCTC TGCTTCCACC AAAACCCTCC CTGACCCCAG GGCTTTTCCT 1260 GATGGCTCCA CTGCTCACCC CACCACACTG TCCCCTTGGC CACCCAATCT CTGTGCCTCA 1320 CTTTCCCTGT TCTTCCTCCC TCCCCCAATA AATGCTGATG TCCCCTGTGG GTGCTCTCTA 1380 GCCCCCCATC TCACAGGCTA 1400
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