| Tag | Content |
|---|
EnhancerAtlas ID | HS023-10167 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr17:5000200-5001500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr17:5000807-5000824 | AAGAACACCATGTACTC | + | 6.81 | | Ar | MA0007.3 | chr17:5000807-5000824 | AAGAACACCATGTACTC | - | 7.2 | | NR3C1 | MA0113.3 | chr17:5000807-5000824 | AAGAACACCATGTACTC | + | 6.8 | | NR3C1 | MA0113.3 | chr17:5000807-5000824 | AAGAACACCATGTACTC | - | 6.94 | | NR3C2 | MA0727.1 | chr17:5000807-5000824 | AAGAACACCATGTACTC | + | 6.39 | | NR3C2 | MA0727.1 | chr17:5000807-5000824 | AAGAACACCATGTACTC | - | 6.49 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I005096 | chr17 | 5000210 | 5001530 |
|
Enhancer Sequence | TCAAACATTT AACTTAAAAA AAAAAAAAAG ACCGAGTCAC TTCCCCAATA ATTTCCTCTT 60
CACCGCACCC CTCAGCTTTT GGAATGAAGC TATGTCAAAA AGACCTGCCT GGGTGAACCC 120
CTGCAAATGG AGGTCAGCTG GACCTCAGTA AAAGCCCAGT GGGAAGGAGC GGGGACGATT 180
CTGGCGATCA CATGAGGAAG GGAGCAGCCT CAGCAGCGCA GGTGGACACA GTCGTCAACC 240
ACTCGCTGGC CGCCTGCGAC GTGAAGCACC TGCGCTGGGC GCGGCGGGTA AGCGCCGACA 300
CTAGCGGGCG CCTGAACAGT CCAGCGGCGT CAGCGCTGCG GAGCAGGAAA GGGTCCCAAA 360
CGCAGGGCGG CCATGCAGCG TGGCGCCCAC CTGTCCCTCT CCTCGAAGCG CTGAGCCAGC 420
ACGATGCACA TAAGGGAAGG AGGAAGGTGG CTTGAGGGCA GTGACCGAGC GGACAGCGGA 480
AGCCCATTTC AGGAGCCCCG GTACCCGAGC TCGGGCCCCT TTCCAATCCC CCAGGCGTCC 540
TTCCCATGTC CTTGTCTCCT AGTCCTGGGA ATCCACGGCC ACTCCACTCT CCTGCAGTAC 600
CGCGGACAAG AACACCATGT ACTCTTCACA GGCAGGTGTC TTCTGGTGGA CCCAACTCTG 660
TTGGTACTTG TCGTCTCCAA AAAGTCCCCA AATGCGCTAG AGGCCAGCCA GCCCGGTATC 720
CGAGAGGTAA GAGCCCCGGC GGCGCAGGCG GAAGCGTGTC TGTCGCGAGG CCTCTCTAGG 780
ACTCCGGGAG GACCCCTCGT TAGCGCAGGA CCTCGGCAGC CGGGGGTTGG GCTCGAGGGC 840
TGAGGGCGGC GCGCCATGCG CGGATTAGCT GCCATCCGGC GGGTCTTTCT GCCGGGGACC 900
AGTGGGGTCG GACGCTGAGG GCCGAGGAAC CCCGCCCCCC CACCGCACCG GGCGGGCTCT 960
GGGGCGTCCG CGGAGGCTCC CGCGTGCGTG TGCGGGGTGG GGTCGGGGTG GCAGTTGGGG 1020
GCAAATCAAT GGGCCTGTAC TTTTGTCTCT CCGCCTGCTG GGATTTGCAG TTTGTGAGGA 1080
CGTTTCACAT CTCACGGATA TTTACGGAGT CCCTTCCACG GCCCAGGCTC TTCTGGACAC 1140
CAAACCAGGC CTAATATAAC TATTTAATAT CTAATTATTA CAATTAAACT TATTTGCAGT 1200
CGGGAAGCAT AGACTCAAAA CACGAAAGGC AGGGTTGGCT TTAGAAAGAA GTCACTGTCG 1260
TCTAAGACTG TCAGAGGGGC TAAGAAGATA GGTATGGAGG 1300
|
