| Tag | Content |
|---|
EnhancerAtlas ID | HS047-20546 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:233367690-233368640 |
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 | GGCGGGAGGG AGGTTTATCC GTAGGAGTCA GCCCAGTTGG GTCAAACTAA GGACCCAGTG 60
CAGACCCCGA GGCCCAGAGA CACAGGTGTG CGCACAAACA CGCACTCTGC GGAAGGCCGG 120
GGCGGGCCTG GCCGCTGCGG GACTCCTGGC CCGGCGCCCT TGACGTCAGC GGCTGGGCCG 180
TGACGTCACC TCACCGCCCC CGCCGCGCTC CCGCCCCCGC CCGCGGGCAC TCAGTCTCCG 240
CTAATGGCAG GCGACGGGGA ATGGCACATC TGTCTTGCCG GGAATTAGTT CATTGAATCA 300
GGCGGCCCGA GCTGCGGCAG CGACCTTAGC CCTGGCCCCA GGGAGGGGTC TGGGCGGGCG 360
GCGTGGGGGA GGTTCAGGCT GGAGGGCTGA GTGCGGGGAC GGGAGGAGGG GACTCACCTG 420
GACTCGCGAG GGGGACTGAG CGCTCTCCAA ATATAGGTCA ATGTCCCGCT CAGCCTCCCT 480
CCCCCAGCAC CGTGAGGACC GAGGCCTGGG GCCTGGCGCC CGCCTGGTGG ACCTCGGGGG 540
CAGGCTGGGG ACCGGGCCCC TGCGGGACGC GGCGCGGCAG GACGCTCCCC GCGCCTTTCT 600
TTCTGCACCT GCCCCTCGGG GTGGGTCCCC CTCTTTACCC TCGCTTCCCC CCGCGGGTGC 660
CGATAAAGGC GGCTAATTCC CGAGCCCGGG GAGGGAGGGG GCGACTGTTC CAGTCAACAC 720
TTCCCCGCGC TCTTCCCCGA CCCTCCCAGA GCGTTCCCGC TGCTCAGGGC GAGGAGCAGC 780
TGCGGCCAGT TTGTCCTAGC GGTTTAGGAG GCAGGGAGGT TTCCTCCAGC CTGGAGCTCT 840
GGCTCGGGCC CTCGGGCCCC AACACCTTCC CGCTGAGACC GCGGGCGTTG TCCCTGGGTC 900
TCTCTGCCTC CATTTCCCCC ACCTCCATTC TGGTTACCCC TTCCCCCCAC 950
|
