Tag | Content |
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EnhancerAtlas ID | HS023-25332 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr9:90407650-90409050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr9:90408373-90408384 | GGTGACTCATC | + | 6.32 | IRF8 | MA0652.1 | chr9:90407971-90407985 | AGTTTCGGTTTCTG | - | 6.64 | JUND | MA0491.1 | chr9:90408373-90408384 | GGTGACTCATC | + | 6.62 | POU4F2 | MA0683.1 | chr9:90408811-90408827 | ATGAATAATTCATGAA | + | 6.33 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 90407699 | 90408115 | chr9 | 90408310 | 90408593 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I087791 | chr9 | 90406569 | 90409354 |
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Enhancer Sequence | AAGAAAAGAA AAGAAAAAAG ACCTTTGGGT GCTTGTCAGC TTCTTGGAAG TGAAGCCAGA 60 CCATTTCCTT GCTCAAGCCA AAGAGCTCAT TGACTCAAGG AGCATCATAG CAACTGGGCT 120 GCATCTAAAA GGGAAGAATC AAGGGCGTGA TCCACAACCA AGGCCTGAGG AAGCAGGGCC 180 CATAGTTGAC CTGCACAGTA TGAGTCATGA CCCATGTGCT GGGGCTCTAG CCATGGGCGG 240 TGCCTCTTGC CATTTCCAGC TTCCTCCTGC AGAGGGTGGG TGTTAACGGT CTTCATTGCT 300 CATAACCTTC TCAAAGGCAC GAGTTTCGGT TTCTGCCTTC CCTGAATCAA GTCTTCTACA 360 TTGCAGTTGC TGTAACAAAA ACTATTAGCA ACAACACAGC ACTACAGAAG CAAGCTCCTT 420 GCTAACAGTG ATTGCTGATG ACATTGTCTT CTAGAGACCA CTCTAGTGGC TCGGCAGCCT 480 TGGTATAGAG CTGATGATAA AAACTTTTCC TGCTTTTGCC AGTCATGAGG AGCATTTCTT 540 TGTCTAGATA AGGGAACTGA AACCCACTGG CCAGCCAGAA TATACTCAAA GCAGTCATTG 600 GGATACGAAT CCCACCATCA TCTCCCATGT TATCCCTTTT GTTACCTTTA AATATGGTCC 660 CATTTACTCA GGACCAATAT TCCCTTATGT GGAGAGCAGG ACTAGTGCCC TTGAGTTACT 720 TACGGTGACT CATCTTTGAG TGGGGAATGT GTTAGTATTT TCAGCAAATG TTAAGTGTGA 780 TGAAACATTT GCTGAACTGT CTCCCCGTTT CGAAATAAGC TAACAGCACT CAGGGGCTCT 840 ATTTACAGCA ATTGGGTGGA GTCAGGAGTG GGAACGCATC TTGCACTGTC ACCTTGATTG 900 ACAATAGCTC TGACCTGTGG AGGATGGTCA AGTCCTGTCT CCTATAACGT GGGGCAGTGA 960 TGGGTCAGGG TCATGGCTCC TGCATTTGGG TGAGGCCTTC TCATCACTTT TAGACAAGCA 1020 AGTTCAGGGT GACCGCAGGC CTCCCCACTT CCATCAGTAT CCTCCCAACT CCCCCTGACC 1080 TCTCTCACGA AGCTCCCCAC CAATTCAGAG ATCCAGTCCT GAGGGGCTAA AAGAAACATT 1140 CATTAACCTG TCTAGAGAGT CATGAATAAT TCATGAATTA CATTGAATTC ATCCCTAGTA 1200 TAACTATCTT CAGAAATTCA GACTTGGTAA CCCGGTAGCC CCCTTCCTCA ATGTCTTTCC 1260 AAGGCCCCAG GTGATCTCTC TGTTCCATAC ATAATGCTTT ACACAGCAAA GTGCTTCTGG 1320 GGGTGGGAGC CCGCTGACCT TCCCTGGAAT CCTGACTGCA GGTTCTGTTT AGAACATGGG 1380 GTCTCATTTT GAGAAGCTCT 1400
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