Variant report

Variant	rs7853326
Chromosome Location	chr9:110662356-110662357
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:110656736..110659365-chr9:110662129..110664911,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10739249	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10759262	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10759264	0.96[ASN][1000 genomes]
rs10759265	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10759266	0.91[ASN][1000 genomes]
rs10816585	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10816586	0.98[ASN][1000 genomes]
rs1339764	0.81[CHB][hapmap];0.88[JPT][hapmap];0.89[ASN][1000 genomes]
rs1339765	0.85[CHB][hapmap];0.82[CHD][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs1416839	0.82[CHB][hapmap];0.89[JPT][hapmap];0.88[ASN][1000 genomes]
rs1929277	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1929279	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1929280	0.84[CEU][hapmap];0.95[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1970403	0.90[ASN][1000 genomes]
rs1999349	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2094919	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2094920	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2104825	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4978644	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4978650	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4978651	0.98[ASN][1000 genomes]
rs7023709	0.85[CHB][hapmap];0.82[CHD][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs7030786	0.82[CHB][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes]
rs7031148	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7040902	0.95[AFR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7047831	0.85[CHB][hapmap];0.82[CHD][hapmap];0.84[JPT][hapmap];0.89[ASN][1000 genomes]
rs7858147	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7873668	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs944473	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs944475	0.85[CHB][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs944476	0.85[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]

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	nsv1051101	chr9:110548257-110697253	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv893701	chr9:110650482-110709587	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 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	chr9:110658000-110668000	Weak transcription	Placenta	Placenta
2	chr9:110660800-110662600	Enhancers	Fetal Stomach	stomach
3	chr9:110661200-110662600	Enhancers	Fetal Intestine Large	intestine
4	chr9:110661600-110670000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:110661800-110666800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr9:110662200-110667600	Weak transcription	Fetal Muscle Trunk	muscle

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