Variant report

Variant	rs10056135
Chromosome Location	chr5:113584657-113584658
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:113583124..113585707-chr5:113637136..113639363,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10036437	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10038352	0.93[EUR][1000 genomes]
rs10038399	0.92[EUR][1000 genomes]
rs10043845	0.93[EUR][1000 genomes]
rs10044601	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10044702	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10053242	1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10061107	0.90[EUR][1000 genomes]
rs10065369	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10078333	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3935351	0.89[EUR][1000 genomes]
rs4072690	0.91[EUR][1000 genomes]
rs4235755	0.89[EUR][1000 genomes]
rs4235758	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4235759	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4270685	0.93[EUR][1000 genomes]
rs4272125	0.91[EUR][1000 genomes]
rs4288107	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4299732	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4308475	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4314390	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4360033	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4376257	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4440350	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4451040	0.88[EUR][1000 genomes]
rs4460131	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4484414	0.93[EUR][1000 genomes]
rs4484416	0.93[EUR][1000 genomes]
rs4484417	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4505939	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4521461	0.91[EUR][1000 genomes]
rs4535442	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs4537054	0.89[EUR][1000 genomes]
rs4558978	0.91[EUR][1000 genomes]
rs4597957	1.00[CEU][hapmap];0.86[CHB][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4705495	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4705643	0.93[EUR][1000 genomes]
rs4705650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4705651	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs5013666	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5022986	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6863368	0.91[EUR][1000 genomes]
rs6865389	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6880768	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6886349	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6887829	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6887986	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6892162	0.91[EUR][1000 genomes]
rs7712075	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7720634	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7731994	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882727	chr5:113548400-113602162	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1029021	chr5:113551892-113599644	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv537865	chr5:113551892-113599644	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113579400-113585600	Weak transcription	Fetal Heart	heart
2	chr5:113581400-113585800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr5:113581600-113586000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:113584600-113586600	Enhancers	Fetal Stomach	stomach
5	chr5:113584600-113587200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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