| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22751 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr7:65878200-65879050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr7:65878538-65878550 | CGTGACGTCACC | + | 6.32 | | CREB1 | MA0018.3 | chr7:65878538-65878550 | CGTGACGTCACC | - | 6.32 | | NRF1 | MA0506.1 | chr7:65878615-65878626 | CGCGCATGCGC | - | 6.02 | | NRF1 | MA0506.1 | chr7:65878616-65878627 | GCGCATGCGCA | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 65878400 | 65878582 | | chr7 | 65878387 | 65878723 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I066413 | chr7 | 65878001 | 65879387 |
|
Enhancer Sequence | AAGGAGCTGG GAAGTTGAGG TGAAACTACT GAGACTGGGT CGCGCCACGT TGCTGAGGCT 60
GCTCTTTAAC TCCTGGCCTG AAGGGATCCT TCCGCCTCGG CCGCATCCAG ACATAGTTTT 120
CTAGTTTTGA CCCACAGAAA CAGTGCTGGG TCGGAGTTTG TCAACTACCC ATCTCCAGAC 180
AGCAACACAA AGGACCTGGC AGGGAGGTCG CGGTTACCAA GCTCCACTCT AAGGAGAAAA 240
CAGCCTAGCT CCAGGCACTG TACCGTCACT GTGACGTCGC GGAAGGCCCG GTGCTGTGAC 300
ATCGCCGAAG ACACGCGCCT TCGGCGAACG CCCGTCCCCG TGACGTCACC AGAGGTGCGC 360
CCAATCGGAA CTCGAGGCGG GGCTGCGGGG GAGGGGGGCC TGGGTCTTCC AGAAGCGCGC 420
ATGCGCAGGC GGGTGGCCAC AGGCAGCTGT CAGCTTCTGC AGGCTCGGAC CCGGCGGCAG 480
GCAACAATAA GCTACAAGGG GAGCTTTACC ACTGCCTGGA TTACTACTAC CTGCGCGTTG 540
GGCGCAGCAA GGGCTTGACG CTACTGGAGC ACGCGCTGCG CACCAACCTG CTGGCGCCCA 600
GCGGGCACAA GCACAAGGTG GCGCAGAAGC TCCTCAATGG ACAGCACAAG CCCGCTAGAG 660
CCAGCTGCAG TCCTTGCCAC GCACTCGCCT CACCTGAGGC TGTGTAGGTG CGGCCCCCAA 720
CACCTAACCC AGCCAGGTAC CGGGGACCAC AGCAGCGTCC CCTGCCGCCC AGCGCCGCTC 780
ATACTGGGCA GGGTTGGCCC CCTCTGAGGC TGCCCCGCAT TAGGGAGCTG CACCCCCTAG 840
CTTGACATCT 850
|
