Tag | Content |
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EnhancerAtlas ID | HS182-08762 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr16:88680250-88681880 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr16:88681137-88681148 | ATTGACCTTGA | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 88680686 | 88681182 | chr16 | 88681563 | 88681625 |
| Enhancer Sequence | GCCGTGTTCT CTTCTAAGAG TTTCATAGTT TTAGCTCTTA CACATAGGTC TTTGATCCAG 60 GCTGGGTGAC AGAGAGAGAC CCTGTCTCAA AAAAAGGGGG GGTGTCGATG AGAGCATGAA 120 CGTTGCTCCG TCTCAGGGTT GGTTTGTGTC ACCGTCCCCG TGGGGGTGAA ATGCAAGGAG 180 GGATCAAGGC AGTTCCTTAT TGGGAAACAG CCCGAGATCC TTCCAGGGCC ATGGCCTGCA 240 GGACTTCCCA GTCAGGAGTC TGTACTTCCA ACTCAGGGAT GTTGTTTGAC TTGGCTCTCA 300 TAAAAATCCA CATTTGGGCC TACACCTTCC AGTAACACTG GACTCCGCTA GACCTGCAGG 360 CATGGGCAGC TTCGTGGCTG GAGCCACACA GTGGCCACAC TTGGAGGGGC CACAGTTCTC 420 ATGCTCCCCT CAGAGACCTG GCAGCCATCA GGACCTGCGA CTGTGGCTCT GGAAGGATTT 480 GCTTTCCACC ACGGGACAAA AACAAGCCCC TTGTCCTCCT CATCTTGTCC GTGTGGCTGG 540 ACGACACCCG CTCTTGTGTA CAGTGGAACA CAAGTCATCT ACGCTTTTCT GAAAGTCAGC 600 TCTCAGGCAG GACTTCGCAG GCCTTTGTTT CAGGGTCACT CATGGCTGTA GCTGCTGCTT 660 AGCCGGTGGC AAGTGCCAGT TTTGACTGTT TTCATTCTCC AGCTCACAGT GAATGGACTT 720 CCCTAAATGT GCTGTATTTG TCATACTTTC CTAACACTAG GCAAAGTAAT CTTCTTAAAG 780 AACATTCAGA ATAAGTGACA TATTTCAGAT GTTTTTAATC CTTTTATGTT ACAGTAATCT 840 CTAAGTTATT TTGAAGTTTA CATGGTCATC CAAACGGGGA AACCGTCATT GACCTTGACA 900 TTGTGCCGCC TTCTTCAGCC TTTCAAGCCC TTTTGGATAG AAGCCCTTCC CCTACAGCAC 960 ACACAGTATT TTCAGTGTGC ACTCAGCCTA AGGCTGCCTT CTCCCCTGAG ACCCCACTGC 1020 AAAGGTGCAG CCCAGCACCC CGTGCACACA CCCCCAGCCG CTCCCTCTGC CCAGATGGGC 1080 TGCCCCCATT TCCTCCATTC CGTCTGCCTG GACGGGCTGC CCCACCTCCT GTTCCCTCTG 1140 CCCAGATGGG CTGCCCCCAC CTCCTCCATT CCCTCTGCGT TTGACAGGCT GCCCCCACCT 1200 GCTCCGTTCC CTCTGCCTGG ACGGGCTGCC CCCACCTGCT CCGTTCCCTC TGCCTGGACG 1260 GGCTGCCCCC ACCTGCTCCG TTCCCTCTGC CTGGACGGGC TGCCCCCACC TCCTCCATTC 1320 CCTCTGCCTT TGACAGGCTG CCCCCACCTC CTCCGTTCCC TCTGCCTTTG ACAGGCTGCC 1380 CCCACCTCCT CCGTTCCCTC TGCCCGGACG GGCTGCCTCT ACCTCCTCCA GGGTTTTGCT 1440 CAGATTCCTC TGCACAGGGA AGTCTCCCCA TCCCCTCCTG CTTGCCAGCC TGCTTTCTTG 1500 TTCCTCATGG CCCTCAGTGC CCATCTGGAG CCCTTGCAGC AGATGGTCCT GGGGCACCAC 1560 CGTCTGCCCT GCTCCCCGTT GCAGCCTCTG TGCCTGTCCC AGAGTCCCGC ACAGGTTGGT 1620 GCTTACCCAC 1630
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