| Tag | Content |
|---|
EnhancerAtlas ID | HS049-06898 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr7:5534260-5535440 |
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 | GAAGGTGGGA AACGGGAAGG GGTAAAAAAG ACGGTGCAGG CGCCGCACCT GCTGAGCTGC 60
AAAGTCACCT CTGGATTTCT CTCCAAAGCA AAAGCAGGAG GCTCCAGACA GCAGGAGATG 120
GAAACGGGGC GTTGGGCAAG GACGGTGCCG TCGTGTGGTC ACTAGGTGGC GATGCGGCTC 180
CGTGCTACCC GCCCCAGATC GCCCCGAGCC TCTGGGGTTA AAAACCAAGT CTGCAGAGCG 240
TGGAAAAAAA ACCTTTTTTC CACGAGATAA CCACATCCAC ATTCTTCCGC CCCGGAGGAA 300
GTCACCTGTC ACAGGTGTTC AGGATGTGGC AGGCCCACGG GAGTGACTGG TCAGGCAGCG 360
GGCCTGGCAC GTCTAAAGCT TCCTAGGCTC CCACAGCACG CCGCCTGGGG CACGGCACCC 420
AGGACGGTGG CAGAGCTGAC CTGACTCGAG TGACCGGCAG CGTCTGCAGG GAGGATGGGG 480
ACGAGGAAAA GGCTCCCACT GCGCCGGGCC TCACCTTTGA GTGAGGATCC AGCCTCCCCA 540
TTCTGCTCCC TGAGGGGGCA CCTGGGTCTC CTGGTGACTC TGTGGGCATG AAAGGTGCTG 600
AGCTCACAGT GCGGGGGCTC CCATCTGGCC ACCCACTGCA CGGGCCGTGA GAGCAGCACC 660
CAGGCCTCCG AGGTGTCCCT AGGGTGGCTC CGGGGCCTGG CTCTGAAAAG GATGGCCCGC 720
TTCTGCCCAG ACGCTGCCCT GGTCACGCTC ACAGCAGCCC GGGTGACTCA GGGTGACACG 780
CTCCCCCGCC CTCCACCGCA AGCAGGGCTT AGCTGGTCTA GGGAAAGAAG GTGTCTTTTC 840
TGCCCAATTT GTAATCCCCT TACTACTGAG GTGTGTCCAA GTCCCAGCCA GAGCGACTCC 900
TTCCTGCACC ACCCCCTCCC TGCCAGGAGC CCCAGCAAGC ACAAAGCTGG GGGTCACGGT 960
GTGGGGGCTG CCAGTGGCAG CAGGTGGCTG GCGTGGGATT CCAAGCTCTG CCACCAAAGA 1020
GACTCCGGCC GCCCCAGGAT GCGGCCTCGG AGCATCGTGC CAGCCTCCAG GGATCCCAGC 1080
GCCGTTTCCT CTGCACAGCT CCTGCCCACG GGCAAGCGAG TGCCACCTGC TCCTTCCACT 1140
GCAGCGTCCG GGCTCCCTTG CCGCAGAAGG CAGGAATCCA 1180
|
