Tag | Content |
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EnhancerAtlas ID | HS092-22150 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr19:1909070-1910700 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr19:1910475-1910488 | GAATGTTCTGGAA | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 1909082 | 1910160 | chr19 | 1910172 | 1910548 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I001909 | chr19 | 1909068 | 1910290 |
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Enhancer Sequence | TCCAGCCTGG GCAACAGAGT GAGACTCTGT CTGAAAAAAA AAAAAATGTG GGCTGGGCAT 60 GGTGGCTTAC GCCTGTAATC CAACCTCAGG CCTGCGGTGC GAGTCTGTGG GGGCAGATGC 120 AGGTGGGGGA AGGCTGGCCA GCTGAGACTG TGGTTTGGGG GTGTTCAGGT GGGGTGGATG 180 CCAGAGATGT GGGAGCCAGA GGCGCTGTCC CCCAGGGCCC TGTGAGCAGT CCCTGCAGGC 240 TGGCTGTCCC CACGCCTGCC TCTCTGCTGT GCTGTCTGCC CGCCTAGGGC AGGCTCCCTT 300 CTAATGGGCG GATCCCGAGA GCTGGGGGCC CCACCAGCCC TTCCTCTCCA GTGGAGTGGC 360 CCTACTGCCT CATGTCCACC TGTGCCAGCA GCAGGGATGG TAATGGCTCT ACTATCTCCT 420 GTCCTCACCT GTGCCAGCAG CAGGGATGGT AACGGCTTTA CTGCCTCCCG TCCTCACCTG 480 TGCCAGTGGC TGGGATGTCT TCACCTGTGC CAGCAGCAGG GATGTCCTCA CCTGTGCCAG 540 CGGCAGGGAT GGTAACAGTG CTGGTGATGT CAGGCCGGGA GGTTCTCACC CGAGAGCCGC 600 CTTGGCACAC TGCCCGGCAG TCAGGGATGT TAGCAGGAGC CCCGGGAGTG ATCCCAGCTC 660 TTCCCGCAGC CCCACTCCAG CCAGGGCCTC CTCTGTGACT GAGTAAGCAG GGACACCCCA 720 GTGGCTGCCT GCTCCACCCG ACAGCCAGGG CCCACCACAG CTGCAGGAAT GTGGTCAAGG 780 GATGGGAAGT CGGGCCCACC AGGGGAGGGG CTGCGCTCCG GGGCTTACGT TTCGTGGCTT 840 GTCTTCTGAG GTCTCTCTTT TCCTAGCCCT TGGCCGACTA GGGGGCGAGT GTTTACAGAA 900 ACCACTGGAG GTGGGTGTTC CGTGTCAGTG CCAGGCTGTG TGCTGTTCTG GGAGGGGGCC 960 CCGTGTCCCC CACACTTGGC ATGCTTGCTT TCTGTCACTG CATAGCAGAC TCCGTGCATC 1020 TGTGGGCTTA ATACAACACC CGCCAGCTCC CGGTTCTGTG GGTCGGGGCC TGAATGTGAC 1080 ATGGCTGGCT CCTCTCTGCG GGGTCTCACC GGGCTGGAAC CCAGGTGTCA GCCAGGGCTG 1140 TGTTGTCATC TGGAGGCTCA ACGGGGGTGG CATCTGCTTG CAACTCACGC AGGCGTTGGC 1200 GGAATTCAGC AGCTTGCGGC CGGGGGACCA AGGGTCCTGC TCAGTTCCTG GCCACATGGC 1260 CCTTCTGTCT GGAAGCCAGG CGCCGCCTGT CCCCGCTTCT GCTTCCAGGC TCTGGCTTCT 1320 GGAGATGCAG AGATCACATC AGTGGTTGCC TGGGTTGCTG TGTGTGTTGT AGGGTGGTGA 1380 GACAAGTTTT CTCTTAGGGG TGATGGAATG TTCTGGAATT TTATAGTGGT GATGGTTGCA 1440 CAACTCCAAG TGTCCTAAGA GCCACTGAAT AGGACACTTG ATAGTTTTTG GTTTTTGAGG 1500 TGTCTTTTTT TTTTTTTTTT TTTTGAGACA GAGTCTCGCT CTGTCACCAG GCTGGAGTGC 1560 AGTGGCACGA TCTCGGCTCA CTGCAACCTC TGCCTCCCAG GTTCAAGCAA TTCTCTTGCC 1620 TCAGCTTCCT 1630
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