Tag | Content |
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EnhancerAtlas ID | HS187-24919 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr9:88337780-88339110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr9:88338266-88338282 | CTTTGTTTACACTGTG | - | 6 | NFKB1 | MA0105.4 | chr9:88338535-88338548 | AGGGAAATCCCCT | - | 6.15 | NFKB1 | MA0105.4 | chr9:88338535-88338548 | AGGGAAATCCCCT | + | 6.1 | Nr2f6(var.2) | MA0728.1 | chr9:88338985-88339000 | GAGGTCAGGAGTTCA | + | 6.22 | REL | MA0101.1 | chr9:88338537-88338547 | GGAAATCCCC | - | 6.02 | RELA | MA0107.1 | chr9:88338425-88338435 | GGGAATTTCC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr9 | 88337886 | 88338800 | chr9 | 88338123 | 88338642 | chr9 | 88338716 | 88338831 | chr9 | 88338800 | 88338819 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I085722 | chr9 | 88337521 | 88338975 |
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Enhancer Sequence | TGTGCTTTTT TTTTGATGTT GATGCTATTC CTTTCTGTTA GTTTTCCTTC TAACAGTCGG 60 GCCCCTCAGC TGCAGGTCTG TTGGAGTTTG CTGGAGGTCC ACTCCAGACC CTGTTTGCCT 120 AGGTATCACC AGCAGAGGCT GCAGAACAGC AAATGCTGCT GCTTGATCCT TCCTCTGGAA 180 GCTTCATCCC AGAGGGGCAC TCACCTGTAG GAGGTGTCTG TCAGCCCCTA CAAGGAGGTG 240 TCTCCCAGTC AGGCTACATG GGGGTCAGGG ACCCACTTGA GGAGGCAGTC TGTCCGTTCT 300 CAGAGCTCAA ACGCCATGCT GGGAGAGCCA CTGCTCTCTT CAGAGCTGTC AGACAGGGAA 360 AATTAGGTCT GCTGAAGCTG TCTGCTGCCT TTTCTTCTGG TAGGCACTGC CCAGAAGTGG 420 AATCTAGAAA GGCAGTAGGC CTTGCTGAGC TATGGTGGGC TCCACCCAGT TCGAGCTTCC 480 TGGCCTCTTT GTTTACACTG TGAGCACAAA ACCACCCATT CAAGCCTCAG CAATGGCGGA 540 CGCCCCTCCC CCACCAAGCT GCAGCATTGC AGGTTGATCT CAGACTGCTG CACTAGCTGT 600 GAGCAAGCCT CCATGGGCGT GAGACCTGCT GAGCCAGGCA CAGGAGGGAA TTTCCTGGTC 660 TGTGGGTTGC GAAGACTATG GGAAAAGCGC AGTATTTGGG CAGGAATGTA CCGTTCCTCC 720 AAGTACAGAC TGTCATGGAT TCCCTTGGCT AAGAAAGGGA AATCCCCTGA CCCCTTGCGC 780 TTCCCAGGTG AGGCGCTGCT TCAGCTTGCC CTCCGTGGGC TGCACCCACC GTCCAACCAG 840 TCCCATTGAG ATGAACCAGG TACCTTAGTT GGAAATGCAG AAATCACCCG TCTTCTCCAT 900 CAATCTCGCT GGGAGCTGCA GACCGGAGCT GTTCCTATTT GGTCATCTTG GAAGCCTCCT 960 CTGGGTTGAC TGTCCTTCTA AAAGAAACCC TAGAGAAAAA GCTCTTCCCT CCCACCATGT 1020 GAGCACACAA TGAAAAGGCA CCATCTATGA ACCATGAAAC AGATCCTCAC CAGATATGAA 1080 TCTGCCAGCA TCTTGATCTT AAACTTTCCA GCCACCAGAA CTGTTAGAAA TAAACATCTG 1140 GCCGGGTACG GTGGCTCATG CCTATAATCC TAGCACTTTG GGAGGCCGAG GAAGGTGGAT 1200 CACTTGAGGT CAGGAGTTCA AAACCAGCCT GGCCAAGATG GAGAAACCCG AACTCTACTA 1260 TAAATACAAA AATTAGCCGG GTGTGGTGGT GAGTACTTGT AATCCAAGCT ACTCAGGAGG 1320 CTGAGGCAGA 1330
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