| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15226 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:12404490-12405500 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr19:12404654-12404674 | CCACACACAAACCCCACACA | + | 6.06 | | RREB1 | MA0073.1 | chr19:12405060-12405080 | CCACATCCCAACCACCCCCG | + | 6.21 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATGGAAGGCT CTGGAAACCA AAAGATTTAC TGTTAGCCCC AAGAGGAGTT AGGATGAAGG 60
GACAGGTCTC AAAGACCCTG ATGCCAATAT CTTTGAAAGC CTCGGAGGAG AAATGGTCGC 120
CCTTGGAAAG AAAGGACTGA AGAGCACAGA GACCACAGCT CCTCCCACAC ACAAACCCCA 180
CACACGAGTC TGGTTTGTGC CTAGTGACCC TCCCACCGTC ACCGTGCAGC CTCCTCACCG 240
GGCTCACAGG AACTGCGAGC CAGGCTGGAG GCGAGATTGC AGTTAGATAT TAACCAGGTG 300
CCCTCAGCCC CGCTGCTTCA CAGGAAGCCG CCTCCCTGAG AGTCAGGTCA CAGCAGACGC 360
TGACCGCCGG CTTCCCCATT GGCCTGGGGA TAAGATCTCT GAGAGTTGCT CAAGAGTCGT 420
CTAAGTTCTT TCTCAGATCT TGAATTCCAG CGGAAAGGCT GGCGCCAAGC AGGCTGAAGA 480
CCCCACAAGG AAGCCCACTC AGCAGCAGAA TGCGGTTTCT TCACCTCCAG TCCCAAGATT 540
CACCCCTCAC TTCTCCACCA ACCAGCGACC CCACATCCCA ACCACCCCCG TCCAGACCCC 600
TAAACACCCC ATCCTCAAAC CTCTCACGGA GGCGGATCTA GGGTGTCCTC TCCTATTAAA 660
CCGTTTCTGC TGCAGCCCTC GGCGTCCGGG TGCAGTGACT TGGGCTGCGA ACCTGTACTG 720
GTTCCGCCGC ACAATCTGGG GAGAAGCGGG GCTGAGGGCG CGGAGCTGCC CAGAGAGGGG 780
CGCCGGGGCC GGGGCCGCAG TCGCAGCTCA GGGACGGGAC AGGACGCCCG GGGTCCCGGC 840
TGCCGGCCCA GCCCCACCCT GCGGCCAAAC GGACCGAGGA CCGAGGTGCG CAGGGGGCGC 900
TCAGGTCCCA GACCCCAAAG ACGCTGCGGC GAGGCCCGGG TCCCGCCACA GCCGGTTCCG 960
ACTGGTTCCG ACCAGCCCTT CGCCCTGCCT CAGGACGCCG GGCCCCGCAC 1010
|
