Tag | Content |
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EnhancerAtlas ID | HS182-16564 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr3:184183700-184184850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr3:184184348-184184363 | GTGTTCAAGGTCAGC | + | 7.21 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 184183759 | 184184052 | chr3 | 184184176 | 184184760 | chr3 | 184184369 | 184184676 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I184464 | chr3 | 184182687 | 184185421 |
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Enhancer Sequence | GCAAGATTGG GCGAGGGGAG GCTCAGATGG CCATGCAAAT AAGACAAAAT CTCTGCCAGC 60 CCAGTGGGGC GGCTCCAGGC AAAGACTGGT AAAGGCTAGG CCCTTGGACT GCCACTGTGC 120 TCAGTTATGG GCTGGGGCTT GCTCCCAAAA TAGGGTGACC TTGGCTCCAA CACTGAGGCA 180 GATCCTGACA AAGCCAACAG CTGGAGGCTG CCTGCCAACC ACACTCCTTG CAGCTGGGCA 240 GCACATCTTT CCTCAAAGGA GGGTCTGGAC AGGACATTTT CCTTGTTACC AGGGGCTCAG 300 ACTCATCAAG AATGAGGGCT AGGGTCACCC CACAGCTAGA CCATGAGGGC CGACAGAGGT 360 GGGAGCTGAG GGCAGGGCAA TTTAGAAGGA ATAGCGGAGG GAGCCAAGCA CCAGTGGTGG 420 CCCTGAGGCC AGTAGCAGTG AATGAGGTCT CTATTTCATG CTCGTAACTT CCCTCTTGTA 480 CAGAGGCCCC CCAGATCCCT GGGGGAGCTG CTCCCCACAT GTGTCCACAT TACCGTGACA 540 TGTGGACTGT GGCAGACATG GGGCTGCTCT GCTCCATTCT CCTTTGAGAA AGTATTGCTG 600 CCCAGCCGCG AGGAGTGTGA TGAGTTGACA GCCTCAGCGT CTGGGCTGGT GTTCAAGGTC 660 AGCTGCAGCT TTTGAGCTGA GATCATGCTC TTCGAGGGGT GGCCCCAGCC AGAGACTGAG 720 CTTGATGATA AGGGCCTGGC TGCTTCTGCC CTGTGAACGA CTCTTCTAAC AGAAAGTCTT 780 GGACACCTTT GTTCCAGGGC TCCCCTGGGG CCGGCCAAGC TTTGTCACAT CTGCACTGTG 840 GTCTGGCAGC TCCCTGCCCC ACCCACCTTT CCTTCCCTTT CCTCTCAGAG GCGTTGCTTA 900 CCAATGAGGC GTGGGTATTC CTGACTCTGT CTCAGCCTCT GCTTCTCAGA GAACTCCGCT 960 GACACAGTCT GCATGGCACA GTCCTCTCTG ATCTCGGAGG ACACCTGTCT TTTTTTTTTT 1020 TTGAGACTGA GTCTCGCTCT GTCTCCCAGG CTAGAGTGCA GGGGCGTGAT CTCGGCTCAC 1080 TGCAACCTCC ACCTCCCGGT TTCAAGCGAT TCTCCTGCCT CAGCTTCCTG AGTAGCTAGG 1140 ATTACAGGCA 1150
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