Variant report

Variant	rs118021499
Chromosome Location	chr10:93501155-93501156
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3420401	chr10:93497972-93502370	Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv975785	chr10:93501141-93525212	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93500600-93504600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:93500800-93501600	Enhancers	Fetal Lung	lung
3	chr10:93500800-93502000	Enhancers	Liver	Liver
4	chr10:93501000-93501200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:93501000-93501400	Enhancers	Stomach Smooth Muscle	stomach
6	chr10:93501000-93501800	Enhancers	Fetal Stomach	stomach

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

Quick links