Variant report

Variant	rs35473722
Chromosome Location	chr8:102877070-102877071
allele	CA/TG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:102876704..102878618-chr8:102883254..102885597,2	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1144545	0.84[AMR][1000 genomes]
rs1148496	0.82[EUR][1000 genomes]
rs1148499	0.81[AMR][1000 genomes]
rs1313944	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs472471	0.82[EUR][1000 genomes]
rs472638	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs473498	0.80[ASN][1000 genomes]
rs477236	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs478069	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs478189	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs478896	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs478917	0.84[AMR][1000 genomes]
rs479041	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs480570	0.84[AMR][1000 genomes]
rs480955	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs481545	0.84[AMR][1000 genomes]
rs485252	0.83[AMR][1000 genomes]
rs485263	0.83[AMR][1000 genomes]
rs485363	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs486196	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs488034	0.81[AMR][1000 genomes]
rs489973	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs490096	0.82[ASN][1000 genomes]
rs490125	0.82[ASN][1000 genomes]
rs494352	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs495636	0.84[AMR][1000 genomes]
rs497905	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs502334	0.84[AMR][1000 genomes]
rs513472	0.84[AMR][1000 genomes]
rs526533	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs529684	0.84[AMR][1000 genomes]
rs531624	0.84[AMR][1000 genomes]
rs540459	0.84[AMR][1000 genomes]
rs544928	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs551295	0.85[ASN][1000 genomes]
rs558159	0.81[ASN][1000 genomes]
rs558772	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs561000	0.82[ASN][1000 genomes]
rs562037	0.84[ASN][1000 genomes]
rs563463	0.84[ASN][1000 genomes]
rs564718	0.81[ASN][1000 genomes]
rs566264	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs566315	0.84[AMR][1000 genomes]
rs566392	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs566501	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs568194	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs569015	0.84[AMR][1000 genomes]
rs569787	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs572692	0.81[ASN][1000 genomes]
rs576173	0.84[AMR][1000 genomes]
rs577756	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs578603	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018653	chr8:102818271-103009082	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv539700	chr8:102818271-103009082	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv518162	chr8:102841031-102893626	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv523850	chr8:102841031-102893626	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv465749	chr8:102847202-102929460	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv611819	chr8:102847202-102929460	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1030076	chr8:102866179-102896458	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102869200-102880200	Weak transcription	Aorta	Aorta
2	chr8:102870000-102891200	Weak transcription	Ovary	ovary
3	chr8:102870600-102879000	Weak transcription	Small Intestine	intestine
4	chr8:102871000-102880400	Weak transcription	Psoas Muscle	Psoas
5	chr8:102871000-102880800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr8:102876600-102879200	Weak transcription	Fetal Muscle Leg	muscle
7	chr8:102876600-102880400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:102876600-102883400	Weak transcription	NHDF-Ad	bronchial
9	chr8:102876800-102879400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links