Variant report

Variant	rs9818626
Chromosome Location	chr3:133809258-133809259
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs11711122	0.81[ASN][1000 genomes]
rs13059653	0.81[ASN][1000 genomes]
rs13065669	0.81[ASN][1000 genomes]
rs13074310	0.84[ASN][1000 genomes]
rs13075472	0.98[ASN][1000 genomes]
rs13080318	0.84[CHB][hapmap];0.90[JPT][hapmap]
rs13080570	0.83[ASN][1000 genomes]
rs28450327	0.84[ASN][1000 genomes]
rs28484700	0.81[ASN][1000 genomes]
rs28667241	0.84[ASN][1000 genomes]
rs34678092	0.88[ASN][1000 genomes]
rs35293292	0.88[ASN][1000 genomes]
rs35702871	0.84[ASN][1000 genomes]
rs35750568	0.84[ASN][1000 genomes]
rs4241372	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4241373	0.98[ASN][1000 genomes]
rs4280634	0.84[ASN][1000 genomes]
rs4305420	0.84[ASN][1000 genomes]
rs4345064	0.81[ASN][1000 genomes]
rs4380411	0.81[ASN][1000 genomes]
rs4413311	0.84[ASN][1000 genomes]
rs4419375	0.84[ASN][1000 genomes]
rs4426678	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4450812	0.84[ASN][1000 genomes]
rs4507252	0.98[ASN][1000 genomes]
rs4507253	0.98[ASN][1000 genomes]
rs4518125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4535222	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4546144	0.80[ASN][1000 genomes]
rs4552343	0.81[ASN][1000 genomes]
rs4558752	0.82[ASN][1000 genomes]
rs4640559	0.82[ASN][1000 genomes]
rs4854610	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4854611	0.86[ASN][1000 genomes]
rs4854614	0.81[ASN][1000 genomes]
rs4854615	0.81[ASN][1000 genomes]
rs4854809	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4854811	0.85[ASN][1000 genomes]
rs4854812	0.86[ASN][1000 genomes]
rs4854817	0.81[ASN][1000 genomes]
rs4854818	0.81[ASN][1000 genomes]
rs4854820	0.81[ASN][1000 genomes]
rs4854825	0.81[ASN][1000 genomes]
rs58282329	0.81[AFR][1000 genomes]
rs62269301	0.90[ASN][1000 genomes]
rs6439460	0.81[ASN][1000 genomes]
rs6439461	0.81[ASN][1000 genomes]
rs6777817	0.84[ASN][1000 genomes]
rs6796570	0.81[ASN][1000 genomes]
rs6802495	0.84[ASN][1000 genomes]
rs7611109	0.84[ASN][1000 genomes]
rs7613782	0.81[ASN][1000 genomes]
rs7632489	0.98[ASN][1000 genomes]
rs7632556	0.97[ASN][1000 genomes]
rs7632691	0.98[ASN][1000 genomes]
rs7653175	0.84[ASN][1000 genomes]
rs9827105	0.84[ASN][1000 genomes]
rs9831998	0.84[ASN][1000 genomes]
rs9842531	0.81[ASN][1000 genomes]
rs9847033	0.81[ASN][1000 genomes]
rs9850689	0.97[ASN][1000 genomes]
rs9853047	0.81[ASN][1000 genomes]
rs9857486	0.81[ASN][1000 genomes]
rs9865639	0.81[ASN][1000 genomes]
rs9867748	0.81[ASN][1000 genomes]
rs9869195	0.84[ASN][1000 genomes]
rs9869613	0.84[ASN][1000 genomes]
rs9870910	0.81[ASN][1000 genomes]
rs9871137	0.81[ASN][1000 genomes]
rs9877506	0.81[ASN][1000 genomes]
rs9884048	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv965344	chr3:133805086-133862489	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133802800-133812000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:133806600-133809400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr3:133806800-133809400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:133806800-133809400	Weak transcription	Placenta	Placenta
5	chr3:133806800-133811400	Weak transcription	Stomach Mucosa	stomach
6	chr3:133808600-133810800	Enhancers	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links