Tag | Content |
---|
EnhancerAtlas ID | HS184-27695 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr7:30469670-30470780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr7:30470651-30470669 | GGCAGGAGGCCAGGAAGG | + | 6.35 | MEF2C | MA0497.1 | chr7:30470532-30470547 | GGGACAAAAATAGAA | + | 6.3 |
|
| 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 |
GH07I030428 | chr7 | 30468170 | 30471016 |
|
Enhancer Sequence | ACAACAAATT GTAAGAAACA CACCATGGGA CAGGAAGTCT GACGTCTCCT TCCAGGTAGC 60 TAGGGAAAGG CAAGGCAGGT TTTAAAGTTA AGAGGCTACC AACATGCAAG AGGGAGGGAG 120 GAGAAACAGT TATGCTGCCA TGAAATAGTT CTCATGAATA GTTCTCATGG GGCTCAGTGG 180 AAAAGCTTTA ATAATGGGGA CTCTGAGAAT GCACCCCATT GTTCTGGGTA GCAGTGATTC 240 AAATGAAACA AAGTTTTCAG CTATCGCTAG GAAGCCAGGC CTCTCCTGAA ATGCTCCCTT 300 GGGCAGCTAC GCTTCTAACC CAACCAGGAA ATAAATGCAT CAAGAGGCTG TAGTGTCTCC 360 GCTTCATCAC AGAGTCATTC CCTGCTCCTG GCTGTTTGTA GAATAGGCTC CTGCTAAACA 420 TGACCCTTAG AAATCCTGGC ACTGACCCAA GAAGGAAGCC CTTACCAGGA AGACGAGGGC 480 CCTATGCTGT CATGAATGAA GAGGACTCCC TCGTGAGAGG CAGTATTGCA GAGCGGGTGC 540 AGCTCCTCTT AAACCCTCCC TCCCCACTGT TCAGCTACAG AACCTTGAAG AAATAAACGC 600 ATCTGTCTGT GCCTCAGTTG TGTCATCTGT AAACTGAGAA TAACTATAAG AGTGCCCCCC 660 ATCCACTGGG TGTGTGAGAT TTCAAGAGGA GGGTATTAGG CACAGTGTCC AGGGGGAAGG 720 GAGCTCTTGT CACTGTTACT GCCCAAGCAC ACAGGACCAC TGGTGGCTGG GCTGCAGCCA 780 GGATCTGGTG CTCCCAGCCA TACCCCACAA GGGCTAGGGC CCCTGGGTTC AATGGCAGAG 840 GTAATGACCT TCCCTTTCAA AAGGGACAAA AATAGAACCA GGAAGTGGGC ACCAAGTTCT 900 GTATTCAGTT ACACTCTGCT GTTTTCTAGT CACCACTTAG GCTTTTTTGA AGGCAGGGAA 960 GGCAGCCTCC AACCAAGATG TGGCAGGAGG CCAGGAAGGA GAGCACCTAA TGCCCCTAAA 1020 AAGCCTGCAG TGTCCAGGCA CATCCACCCA CTCGGGCTGC CTTCACTAGG GCCAGTGCAG 1080 GTTGGGAATG CACAAAGCAG CCAAGACTCT 1110
|