| Tag | Content |
|---|
EnhancerAtlas ID | HS080-02311 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:159753070-159754170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:159753749-159753769 | CCCCCATCCACCCCTCCCCC | + | 6.32 | | ZNF263 | MA0528.1 | chr1:159753748-159753769 | TCCCCCATCCACCCCTCCCCC | - | 6.86 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGCATATATC CGCCCAATGG ACTCTTTACT GTAGGTCTGC CTGTGGTCTT TTCTGCAATA 60
GCAGGCTGAA TAAGATAGAA ATTCACCATA AAATATGTGA GTTCCTGTAC GTACCTGTAT 120
GAGTTCTGTT AGATCTGGAG GCCGCACAGT GGAATGAGAC ATAATTCCTG CTCTCAGGAG 180
CTCAGCCTGC TGGAGAAGAT GGGCACAGAT AGAGTCCACC ACAGACAATG GATGCTATTG 240
TAGACATGCA TTCCAGTTCC AGTGGAGACA TAGAAGAGTG GGGAGTCAAG GGTTCCCCTG 300
TAGATCTCAT CTTTTGTATC ATAGACCAGA GACAGGCCTA GCCAACTGGT CCTCCTTTCT 360
GCTGCTTTCC CCCTTCCACC ACTAACCACC CAGTTCATCC CTGTCCAACT CAACCTTAAA 420
CAAGAGATAT CAGCTGAAGT CTTGCCAATC TAAGGCCATA AGATGCCCTC TCCCCAGTTT 480
AACTTTATTT GTCAAATCTG AGTGATCAGT TCCTTCAAGC TTAGTCTCCA CCTAGCCTAC 540
TCAAGTGAGG ATGTCTCCCA AAGAGAAGAA ACCCACACAT TCCAGGCATT CCAGCTGCAA 600
CAGAGGAATG AGAATGCAAA TAGAGGATGC ACTGAAACCC TTACCCTCCT GTCACCAAAA 660
GTTCTGTCTA CCCTGCTCTC CCCCATCCAC CCCTCCCCCA ATAGTATGGC CCCATTCTGT 720
TTCTGATGCA AACCAGAACA TCTTCCAAAG GGGTGTGTGT GTATTTTCAT GTGAAGGGAG 780
TAGGGCATGA AGGGTGTGAA TGGGCCACTT CCTGAACCTC TCCCCTCCAG TCGGAGGGCT 840
TACCAGGATG GAGAGAGAGA GAGAGAGGTG TGAGGCATGA AGCTTCCCCA AGTTCGTGTC 900
TCCACTCTGA TCCTCACCTG CTAGGCCATA CAACCAATCC TTGCCCTTTC TGCCTCTGTT 960
CCTGTGTCAC TCCATCCTCC CCACATCTCT GCACTGTGGA AGAGGAATAT GCCCTTCCCT 1020
TCCTCCCAAG GCTCCTGCAA GGGAAACAAA ATTTTGCTAA CCCCATTAAA GCCCTGTGTA 1080
CTGCCTCCAT CCCCATAATT 1100
|
