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Variant report
Variant
rs373255263
Chromosome Location
chr6:37390005-37390006
allele
A/T
Outlinks
Ensembl
 
UCSC
Chromatin state
Related regulatory elements
Target genes
Other information
TF binding region (count:0)
CpG islands (count:0)
Chromatin interactive region (count:5)
LncRNA region (count:0)
Mature miRNA region (count: 0)
miRNA target sites (count:0)
No data
No data
(count:5 , 50 per page) page:
1
No.
Distal block
Cell Line
Cell type
Cell Stage
1
chr6:37389971..37393834-chr6:37440150..37443110,4
MCF-7
breast:
2
chr6:37388900..37391581-chr6:37403584..37406042,2
MCF-7
breast:
3
chr6:37384249..37387029-chr6:37388839..37391579,3
K562
blood:
4
chr6:37383701..37387029-chr6:37388839..37391915,5
K562
blood:
5
chr6:37322263..37324339-chr6:37389226..37391465,2
MCF-7
breast:
No data
No data
No data
Variant related genes
Relation type
ENSG00000137200
Chromatin interaction
Extended variants information (count: 1 )
Associated traits (count: 0)
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
No.
Variant name
Chromosome position
Chromatin state
Related regulatory elements
Target genes
Extended variants
Associated traits
1
esv1807065
chr6:37379409-37399185
Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'
TF binding regionCpG islandChromatin interactive region
5 gene(s)
inside rSNPs
diseases
No data
Chromatin state (count:0 , 50 per page) page:
No data
Quick Search:
Input of quick search could be:
dbSNP/dbVar ID:
rs12345
/
nsv7879
a single nucleotide as 0-based coordinates:
chr1:12345
chromosomal regions:
chr1:12345-34567
what's new
New variant types
New dimension of annotation
New regulatory manner
More detailed annotation on variant overlapped TFBS
More extended data
New search manner
Quick links