Tag | Content |
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EnhancerAtlas ID | HS023-13957 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr2:26963200-26964690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr2:26963620-26963630 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr2:26963620-26963630 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr2:26963620-26963630 | AATGGAAAAT | - | 6.02 | NR2F1 | MA0017.2 | chr2:26963532-26963545 | CAAAGGTCAATGG | + | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 26963213 | 26963516 | chr2 | 26963762 | 26964154 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I026740 | chr2 | 26963801 | 26963950 |
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Enhancer Sequence | TTATGTCAGT TTTATCTCAA AGAAGCTGTT TAGGAAAAAA CAAACCATAG AGGCTTTGCA 60 CACGGCCCAG CAGATGAGCT AAGCACTCCC ACCTACACCC ATTTTGTTCT GATGGCCACG 120 GTAGGGGGTG TAAGTCCCCC ATGCCTCTTT ATGAGAGGGT CAGCGGGGAG GCCATCAATG 180 CTTCTGGTCA ACTTCTGCCC ACCCCAGACC AGGCCAGCTG TCGGCACAGG TGTCGCTAGT 240 GTCACTCGAA GCTGGACACA TATCAGTATA TGGATGTAAC AAGCAACCAT GAGGTCCCCA 300 TGGGGTGTTG CTGGCACAAG CCAGACATCA AGCAAAGGTC AATGGGGCAG GAGCTAATCT 360 AAAACACTGT GCCTCTGCCT AGGCAAACAG GGTCTCTCAG GCCCTAGCAG GCTGAGGGTA 420 AATGGAAAAT CCCCAGAGCC CATGAAACCC CATTTCTTTG GCTGTTTCTT CGCCTATTAA 480 AATTACTCTC CCATCTTTTT CGAGGAGTCC CAAAGGGTCT CATCCCATCT AAACCACTAT 540 GGGGTAACCT CTGCCTAGGC TGGCACGCAC ACCAGGGTGA GGGACAAGGC GCCATGTGGC 600 CCAATCGTTC TGCCACCTGC CGCTTGGGGC TGGAGCTGCT CAAGGAGACA GGCTCCTCCT 660 CGCCTACAGC TGTCAAGACA GGCGGACCAT CCTGCTGCTC AGGCTGCAGA GTCTGCCCCA 720 ATGAGCACAG TCCTCAAACC CCACCCACCT ACTGTGACAC TCCCTCCTGC AACTTCAGAG 780 CATGTTGTCT GGTGCTCCAA ACTTTCGTGG TGGGTTTAGT GAAAACGCTT TGGATTTGTA 840 CTCACAGCCC CCTCTCTGTG ACTTAGCCCT CTCTCCTGAG TGCATGAGGA CTGGGCTGTG 900 TGGCAGGAAC CATACAAACC TCAGTGCTAT GCTCTGCTAT GCTTTTATTT CCCTTGTGGT 960 CTGCCTGCTT CCCTTCAGAT GAGGCTGGCC AAGAAGCACC ACAGACCCTG ATGCAAAATT 1020 GCCCCTAAAG CACTTCAGCC CGACCAGTCA GGTCTGCATT CCTGGATAAG CCCAATGCTG 1080 ACCCCATGGG GACCCCCACT CCCTTCTCCA GTACTAGGAG CTGGGCCCCA GGGAGGGACT 1140 TGGATAGGAC CCGCTCGTGT CTGCCACCAT GAGTGTGAGC ACAGGGCTGA TGGAGCTTTG 1200 CAGAGAGAAA TGAAGGTCAA GGTGTGTGGG CTGAGTGCCA AGTGAGACAG AGAGGGCTCC 1260 AAGGCTGGGG AGGTGTGGAC ATGGGGCCGG GGCTGGGCCT GACTGAGCCT GGAAGGAATG 1320 GTGGGATCTA GCACATGGCA ACAGCATTTC AGGTGTAGGA AATTGAGCAA AGGCCCCATA 1380 GGGGAATGTT CCCAGAGTGC TGGAGAACAG TGAGAAGAGC CCGGGGATCT CCTTAGGAAG 1440 GGGAGGGAGT GGGCTCCATG AGTCCGGGGC TGTGTCCATC TCATTTGTGG 1490
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