| Tag | Content |
|---|
EnhancerAtlas ID | HS187-10050 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:7892990-7894050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr17:7894015-7894030 | GAGGTCAAGAGATCG | + | 6 | | Zfx | MA0146.2 | chr17:7893993-7894007 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH17I007989 | chr17 | 7892601 | 7894309 |
|
Enhancer Sequence | GGCATGCTAG CGCATGGCGG AGGTTGCAGT GAGCCGAAAT CGCGCTATTG CACTCCAGCA 60
TGGGTAACAA GAGCGAAACT CGGTCTCGGA AAAAAAAAAA TCTGTTCCAG CAAATGATAA 120
AGCTGGAGAG AATGTTACTA ACAGAACTGA AAATCTGAGG AATTTGAGGA AATGTGTTCT 180
TCGTTGAGAG CAAAGTCACG CAGTGCTGAG CTGAGCACCC AGCGCAAAGG AGGGGCTCCC 240
TAAAGGAAGG TGGAAAGGTC TCCCCAGTAG AGCTCCGCCC AGCCCCAGCT CTAAGCAGCG 300
GGCCCCGGGC ATCAGGGTTT CAGGGCTGAG GAATGTCCAG CGCCGCCCGA TCGCGCCTCG 360
CTTCCTCCAT CACTAAACCA CCGGGGGACT GACTGCCCGA GGCTGGTGCA GAAGCGGGTG 420
CGGAAGCGGG AGAGGGAACG CGCGTGGCGC TCCAGCCGCC ACCCCAACCC TGCCACTTCC 480
GCAGCTGCCC GGGCGCCGCT GCACCCGGAC CACTCTGCGG TCTACCCGCT GCGGCCAGAA 540
GAAGAGAGAC TCCGGGGAGG GTGGCCCTGC CGCACCCTGG CCTTCACAGA GCAGGGGGCG 600
GAAGAGCCCA GGTGCCCTCG GTGCCTGCGC AACCTGAGCC CCGGCCGCCT CGCGCCTTAT 660
CCTTGGGGCT CCCCCTGGCG GCTAAGCCGG TCCCTGCAGG GAAACGTGCC CGTTGTCTCA 720
TCTGCATCCA CTTAGCACCA AGACGGGGTA GCTGAGGGGG TCGGCGGAAG AGGAGAGGGG 780
AGGCAGCAAA AGATGATCCA TGCGGACGAC CAGGGAGCCC ACACCAGCCT CCAAGCGCGT 840
CAGCCTCCAG CTCCACTCCC CAGGGTGAAG AGTCAACGGA CAATCACCCC GAAGTAAGGC 900
CCTACCGCCT CCTGAAAAAG GTGGTTAAAG AAGGGCAATC CGCTAAAGAA TAGAGTACAC 960
GGGCCGGGCG CGGTGGCTAA CGCCTGTAAT CCCAGCACTT TGGGAGGCCG AGGCGGGCGG 1020
ATCACGAGGT CAAGAGATCG AGAGCATCCT GGCGAACACG 1060
|
