| Tag | Content |
|---|
EnhancerAtlas ID | HS080-16827 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr19:12404440-12405500 |
Target genes | | Number: 18 | 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 | CTGACAAAGG GTTCATAACG TTACTGGGAA TTGAGGAGTG AAGTTAGCAT ATGGAAGGCT 60
CTGGAAACCA AAAGATTTAC TGTTAGCCCC AAGAGGAGTT AGGATGAAGG GACAGGTCTC 120
AAAGACCCTG ATGCCAATAT CTTTGAAAGC CTCGGAGGAG AAATGGTCGC CCTTGGAAAG 180
AAAGGACTGA AGAGCACAGA GACCACAGCT CCTCCCACAC ACAAACCCCA CACACGAGTC 240
TGGTTTGTGC CTAGTGACCC TCCCACCGTC ACCGTGCAGC CTCCTCACCG GGCTCACAGG 300
AACTGCGAGC CAGGCTGGAG GCGAGATTGC AGTTAGATAT TAACCAGGTG CCCTCAGCCC 360
CGCTGCTTCA CAGGAAGCCG CCTCCCTGAG AGTCAGGTCA CAGCAGACGC TGACCGCCGG 420
CTTCCCCATT GGCCTGGGGA TAAGATCTCT GAGAGTTGCT CAAGAGTCGT CTAAGTTCTT 480
TCTCAGATCT TGAATTCCAG CGGAAAGGCT GGCGCCAAGC AGGCTGAAGA CCCCACAAGG 540
AAGCCCACTC AGCAGCAGAA TGCGGTTTCT TCACCTCCAG TCCCAAGATT CACCCCTCAC 600
TTCTCCACCA ACCAGCGACC CCACATCCCA ACCACCCCCG TCCAGACCCC TAAACACCCC 660
ATCCTCAAAC CTCTCACGGA GGCGGATCTA GGGTGTCCTC TCCTATTAAA CCGTTTCTGC 720
TGCAGCCCTC GGCGTCCGGG TGCAGTGACT TGGGCTGCGA ACCTGTACTG GTTCCGCCGC 780
ACAATCTGGG GAGAAGCGGG GCTGAGGGCG CGGAGCTGCC CAGAGAGGGG CGCCGGGGCC 840
GGGGCCGCAG TCGCAGCTCA GGGACGGGAC AGGACGCCCG GGGTCCCGGC TGCCGGCCCA 900
GCCCCACCCT GCGGCCAAAC GGACCGAGGA CCGAGGTGCG CAGGGGGCGC TCAGGTCCCA 960
GACCCCAAAG ACGCTGCGGC GAGGCCCGGG TCCCGCCACA GCCGGTTCCG ACTGGTTCCG 1020
ACCAGCCCTT CGCCCTGCCT CAGGACGCCG GGCCCCGCAC 1060
|
