Variant report

Variant	rs35175011
Chromosome Location	chr8:89352411-89352412
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10100170	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1012116	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10504845	1.00[CEU][hapmap];0.84[CHD][hapmap];0.83[LWK][hapmap];0.88[MKK][hapmap];0.97[TSI][hapmap];0.97[EUR][1000 genomes]
rs11774961	0.87[ASN][1000 genomes]
rs13250349	0.87[ASN][1000 genomes]
rs13256784	0.83[EUR][1000 genomes]
rs13261175	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13262875	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1394511	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1504801	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16881203	0.94[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs16881281	0.81[CEU][hapmap]
rs16892543	0.97[EUR][1000 genomes]
rs1910730	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28787399	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34051963	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35660410	0.89[ASN][1000 genomes]
rs4246109	0.85[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs4246111	1.00[CEU][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs4369037	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4395935	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4461943	0.96[ASN][1000 genomes]
rs4497011	0.96[ASN][1000 genomes]
rs4604492	0.87[ASN][1000 genomes]
rs4961095	0.89[ASN][1000 genomes]
rs56231945	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58255283	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58418586	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58644813	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6469364	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6469372	0.96[ASN][1000 genomes]
rs67312178	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6984041	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6989402	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6992417	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs6994283	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7002751	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7003388	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7004601	0.96[ASN][1000 genomes]
rs7006944	0.96[ASN][1000 genomes]
rs7823223	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7825672	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029898	chr8:88837956-89606641	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1030028	chr8:89060085-89733470	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1019111	chr8:89186908-89475460	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv831386	chr8:89209788-89403546	Enhancers Genic enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv891171	chr8:89342944-89439469	Enhancers Weak transcription Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs35175011	ARHGEF16	trans	parietal	SCAN

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89350800-89352600	Enhancers	Fetal Lung	lung
2	chr8:89352200-89352600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:89352200-89352600	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr8:89352200-89352600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:89352200-89352600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:89352200-89352600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr8:89352200-89352800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:89352200-89352800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:89352200-89352800	Enhancers	Colon Smooth Muscle	Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links