| Tag | Content |
|---|
EnhancerAtlas ID | HS076-04196 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:159753180-159754140 |
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 | GTACCTGTAT GAGTTCTGTT AGATCTGGAG GCCGCACAGT GGAATGAGAC ATAATTCCTG 60
CTCTCAGGAG CTCAGCCTGC TGGAGAAGAT GGGCACAGAT AGAGTCCACC ACAGACAATG 120
GATGCTATTG TAGACATGCA TTCCAGTTCC AGTGGAGACA TAGAAGAGTG GGGAGTCAAG 180
GGTTCCCCTG TAGATCTCAT CTTTTGTATC ATAGACCAGA GACAGGCCTA GCCAACTGGT 240
CCTCCTTTCT GCTGCTTTCC CCCTTCCACC ACTAACCACC CAGTTCATCC CTGTCCAACT 300
CAACCTTAAA CAAGAGATAT CAGCTGAAGT CTTGCCAATC TAAGGCCATA AGATGCCCTC 360
TCCCCAGTTT AACTTTATTT GTCAAATCTG AGTGATCAGT TCCTTCAAGC TTAGTCTCCA 420
CCTAGCCTAC TCAAGTGAGG ATGTCTCCCA AAGAGAAGAA ACCCACACAT TCCAGGCATT 480
CCAGCTGCAA CAGAGGAATG AGAATGCAAA TAGAGGATGC ACTGAAACCC TTACCCTCCT 540
GTCACCAAAA GTTCTGTCTA CCCTGCTCTC CCCCATCCAC CCCTCCCCCA ATAGTATGGC 600
CCCATTCTGT TTCTGATGCA AACCAGAACA TCTTCCAAAG GGGTGTGTGT GTATTTTCAT 660
GTGAAGGGAG TAGGGCATGA AGGGTGTGAA TGGGCCACTT CCTGAACCTC TCCCCTCCAG 720
TCGGAGGGCT TACCAGGATG GAGAGAGAGA GAGAGAGGTG TGAGGCATGA AGCTTCCCCA 780
AGTTCGTGTC TCCACTCTGA TCCTCACCTG CTAGGCCATA CAACCAATCC TTGCCCTTTC 840
TGCCTCTGTT CCTGTGTCAC TCCATCCTCC CCACATCTCT GCACTGTGGA AGAGGAATAT 900
GCCCTTCCCT TCCTCCCAAG GCTCCTGCAA GGGAAACAAA ATTTTGCTAA CCCCATTAAA 960
|
