| Tag | Content |
|---|
EnhancerAtlas ID | HS007-09813 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr2:233367760-233368350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | + | 6.32 | | CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | - | 6.32 |
|
| | 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 |
| GH02I232500 | chr2 | 233365404 | 233368709 |
|
Enhancer Sequence | GGCCCAGAGA CACAGGTGTG CGCACAAACA CGCACTCTGC GGAAGGCCGG GGCGGGCCTG 60
GCCGCTGCGG GACTCCTGGC CCGGCGCCCT TGACGTCAGC GGCTGGGCCG TGACGTCACC 120
TCACCGCCCC CGCCGCGCTC CCGCCCCCGC CCGCGGGCAC TCAGTCTCCG CTAATGGCAG 180
GCGACGGGGA ATGGCACATC TGTCTTGCCG GGAATTAGTT CATTGAATCA GGCGGCCCGA 240
GCTGCGGCAG CGACCTTAGC CCTGGCCCCA GGGAGGGGTC TGGGCGGGCG GCGTGGGGGA 300
GGTTCAGGCT GGAGGGCTGA GTGCGGGGAC GGGAGGAGGG GACTCACCTG GACTCGCGAG 360
GGGGACTGAG CGCTCTCCAA ATATAGGTCA ATGTCCCGCT CAGCCTCCCT CCCCCAGCAC 420
CGTGAGGACC GAGGCCTGGG GCCTGGCGCC CGCCTGGTGG ACCTCGGGGG CAGGCTGGGG 480
ACCGGGCCCC TGCGGGACGC GGCGCGGCAG GACGCTCCCC GCGCCTTTCT TTCTGCACCT 540
GCCCCTCGGG GTGGGTCCCC CTCTTTACCC TCGCTTCCCC CCGCGGGTGC 590
|
