Tag | Content |
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EnhancerAtlas ID | HS103-26250 | Organism | Homo sapiens | Tissue/cell | HUES64 | Coordinate | chr9:138089650-138091960 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr9:138089928-138089941 | TTCTGGAAGGTTC | + | 6.19 |
| | 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 |
GH09I135198 | chr9 | 138090701 | 138091010 |
| Enhancer Sequence | CTGGGCAGTA GCAGAGGCGG CGGCCAGGGC CCTGTTGAGC CACGTCGCGT CCCTGAGCTG 60 GGCTGTGTTC TCTGCACTAA GAGCTGTAGG GGTTCCCTCC TTTAGAGGAC AGACCTGTGG 120 GTTTTACAAG GTGTGGGGCC AGAACCCACT CACAGCAGCA ACTGACTCAG GGGCTCAGGC 180 AACGACTTCT CTGCTCTTTC TCTTTCCCAT GCACAGAGAG CACAGCCTCA CTTTCTTACT 240 CTGCAAAGGA GATGGAATTG TCTCCAGCCA AATCAAACTT CTGGAAGGTT CCTAAAGCCA 300 CCTGGCTCAA GCTACGTTGC ACCCTCCCAC CGGGATGCTT TTCCTCTTTC TCCCTTTCGT 360 CGACTCCTCT TCATCCTCCG AACACCACCT TAGCCCATTC CCCAGGAAGC CTTCTCAGCC 420 CCCGCCTGGC TGACACATAC CAGGTGGCGC AGGCACCCGA ACCTGGGTGT GGGTGCACCG 480 CACGGAGGTT TAAATCGCAG CTCCACCCCT TGCAGCCACT GCTCTGAGCC CCTACCGGCA 540 GGCGGGGAGA GGCAGGAGCC ATCCTCACAG GCCCGCCTCG CCTCCCTCTG TGGATCCTGT 600 TTCCCCACCT CCCTAAAAGT GGATCCTGGG CCTCTTCCTT CGGAGCTTCT GCCCTGTCAC 660 TTAACTGCTG GCTTCATGTC TGTCTTGAGT AACTCCTCCA GGGTGGAGAC GGTGTCTCCT 720 GTGACTGTGT CCCTTTGAGC ATCACCCTGA GCCCTGCACA CTGCAGACTG TGAGTGAGTA 780 AGGGATAGCT GGGTGAATAG GTGGTCCTGC AGCCAGAACC CCCATTGAGG GCCCCGCTTT 840 GACATATAGA CCCCTGGGAT CTTAGGCCTC CAGATACCCT GATCTCTGCA TCCCACAGGA 900 ACCTGTAGAC CACCCGACAC CAAAGGGAGA GCAAGCCAGG GCTCAGAGCC ACTGCAGTCC 960 ATAACTCACA GGCCACTCAA TTAATGACCC ATGGCAGAAG CATGGTGAGT GCAGCCGCCT 1020 CTTGGAAGCC ACCCCCCGTG TATACAGCAC TTGGATTTGT TAAAATATTG AATCTGTTAG 1080 GTGGAAAATG AAAAATGCTA GATGAGCCGC TCTTCAGTCT GGCCTCGGGC ACATCATGGG 1140 AGAGCAAATG CAATCTGCCC CGCCTCACTG GCTCGTTCAG CCCAAGATTA ATGGCAGAAG 1200 GGTCTGGAGA GGGGCAGGTC TCCAGGCTGG CCGGCTGGAA ACCGGTGAAA TACGATGGTT 1260 TGTAATCTGT GTACTTGTCA TGTAAATGAG TGTCCTCAAA GGGCTCTTAC ATGTGTCTTG 1320 GCTTCCATGC AGAAAGCTGA AAGCACCAGA CTGAAGGAGG CATTCATCAT CCGATCATCC 1380 GACAGGTGCA GCTCCGCAGC CCAGAGGTGC CACCACATCC TTCAAGGGCA GATGCGGGGC 1440 TTTCTTCTCC CTTCGCAGAG GGGAGGCAGG TGCCTGGGGA ATTCGTGTGG CCATAGCTGC 1500 AGCACTGGGG AGGGTTAGCC ACCCCCTCCC CCACCCAGAC CATGGATTTT ACCCCCTGGG 1560 GAGGGTAACT GGGAGAAAGG AAGCCAGCCC TAGGAGACTC AGCATGCCTG GGAGTTAGTG 1620 AAATCAGCCT CTTAGATCTA TTTTCCAGCA TGTTCTGTTG ACAGGGACAA GAAGGCTGAT 1680 TTTTGAGAGC TGCTTGGGTG TGGCATAGAT TGGACATCGG TAAGGACTTC CATCAGACCT 1740 GTCTTGAATG GCAAGGAGAG GTTTTGCAGC TGGTCTTCCT AAAAGGCTAG AGAGTCCCCA 1800 TGCCTGCTAG ACCAGGGAAG GCTGGCAGAG TGCGGAATGA AGATGGAAGG GATGAAGGTG 1860 GACAGCCAAA TTTGGCTCCA GTCCTCTCTT CTCGTGCTGT ACCCAGGACA GACATCACTA 1920 AGCAATCAGC CACTCATTCC TGCCGAGCCC AGCAAGGACA GCAGATGCCT CCTCCACACA 1980 GCTCCTGGGC TGTAAGCAAT ATAAGCTGAC ATTGACTAGC TTAAGCCGCA CAACCTAAGC 2040 AATAATGGCA AAAGGCAATG GGCTTGCTGG GGGACATGAG CAGTTCACAG TGTCCCCGCC 2100 AACACTGAAG AGCGGGACTC AACAAGGACA GACCCTGGAG CAGCTCCAGG GGTCCTGGGA 2160 CCACCACTCA GATTCTCCAG AGGAAGGGTC ACTGCCAGGA TGCCTCCTCT CCAGCCATGT 2220 CTGACCCTTG TGTCTATCCT CTCAAGCTCA GGCTCTGGGG AGGAGAATGT GCAGCTGGGG 2280 CCATGTGCTC ACCTCTGGCC AGGTGAGGGC 2310
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