Variant report

Variant	rs35169611
Chromosome Location	chr8:96286893-96286894
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11776206	0.91[ASN][1000 genomes]
rs11777463	0.95[ASN][1000 genomes]
rs16893808	0.94[ASN][1000 genomes]
rs35084958	1.00[AFR][1000 genomes]
rs35234362	1.00[AFR][1000 genomes]
rs35526423	1.00[AFR][1000 genomes]

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	nsv1023866	chr8:96273255-96306378	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96285400-96287000	Enhancers	Fetal Muscle Leg	muscle
2	chr8:96286000-96287000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr8:96286000-96287200	Enhancers	Fetal Heart	heart
4	chr8:96286200-96287000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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