| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22337 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr7:5534360-5535270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr7:5534415-5534434 | TGGTCACTAGGTGGCGATG | + | 6.16 | | FOSL2 | MA0478.1 | chr7:5535020-5535031 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr7:5535020-5535031 | GGGTGACTCAG | + | 6.02 | | PAX5 | MA0014.3 | chr7:5534998-5535010 | CTGGTCACGCTC | - | 6.18 | | ZNF263 | MA0528.1 | chr7:5534729-5534750 | GGAGGATGGGGACGAGGAAAA | + | 6.78 |
|
| | 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 |
| GH07I005494 | chr7 | 5533861 | 5536223 |
|
Enhancer Sequence | GCTCCAGACA GCAGGAGATG GAAACGGGGC GTTGGGCAAG GACGGTGCCG TCGTGTGGTC 60
ACTAGGTGGC GATGCGGCTC CGTGCTACCC GCCCCAGATC GCCCCGAGCC TCTGGGGTTA 120
AAAACCAAGT CTGCAGAGCG TGGAAAAAAA ACCTTTTTTC CACGAGATAA CCACATCCAC 180
ATTCTTCCGC CCCGGAGGAA GTCACCTGTC ACAGGTGTTC AGGATGTGGC AGGCCCACGG 240
GAGTGACTGG TCAGGCAGCG GGCCTGGCAC GTCTAAAGCT TCCTAGGCTC CCACAGCACG 300
CCGCCTGGGG CACGGCACCC AGGACGGTGG CAGAGCTGAC CTGACTCGAG TGACCGGCAG 360
CGTCTGCAGG GAGGATGGGG ACGAGGAAAA GGCTCCCACT GCGCCGGGCC TCACCTTTGA 420
GTGAGGATCC AGCCTCCCCA TTCTGCTCCC TGAGGGGGCA CCTGGGTCTC CTGGTGACTC 480
TGTGGGCATG AAAGGTGCTG AGCTCACAGT GCGGGGGCTC CCATCTGGCC ACCCACTGCA 540
CGGGCCGTGA GAGCAGCACC CAGGCCTCCG AGGTGTCCCT AGGGTGGCTC CGGGGCCTGG 600
CTCTGAAAAG GATGGCCCGC TTCTGCCCAG ACGCTGCCCT GGTCACGCTC ACAGCAGCCC 660
GGGTGACTCA GGGTGACACG CTCCCCCGCC CTCCACCGCA AGCAGGGCTT AGCTGGTCTA 720
GGGAAAGAAG GTGTCTTTTC TGCCCAATTT GTAATCCCCT TACTACTGAG GTGTGTCCAA 780
GTCCCAGCCA GAGCGACTCC TTCCTGCACC ACCCCCTCCC TGCCAGGAGC CCCAGCAAGC 840
ACAAAGCTGG GGGTCACGGT GTGGGGGCTG CCAGTGGCAG CAGGTGGCTG GCGTGGGATT 900
CCAAGCTCTG 910
|
