Variant report

Variant	rs13171462
Chromosome Location	chr5:119911812-119911813
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	chr5:119906837..119908623-chr5:119910419..119912812,2	K562	blood:
2	chr5:119901221..119903356-chr5:119911285..119913616,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10042359	0.90[JPT][hapmap]
rs10051708	0.84[ASN][1000 genomes]
rs10059446	1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10062601	0.88[JPT][hapmap]
rs10063554	0.88[JPT][hapmap]
rs10063637	0.88[JPT][hapmap]
rs10063663	0.90[JPT][hapmap]
rs10063718	0.88[JPT][hapmap]
rs10069225	0.90[JPT][hapmap]
rs10069331	0.90[JPT][hapmap]
rs10069634	1.00[CEU][hapmap];0.90[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10069672	0.90[JPT][hapmap]
rs10069800	0.90[JPT][hapmap]
rs10074464	0.90[JPT][hapmap]
rs10076191	0.88[JPT][hapmap]
rs10077688	0.88[JPT][hapmap]
rs10079794	0.90[JPT][hapmap]
rs10440773	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10478475	0.90[JPT][hapmap]
rs10478476	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs10478477	0.88[JPT][hapmap];0.84[ASN][1000 genomes]
rs10478478	0.82[YRI][hapmap];0.82[AFR][1000 genomes]
rs10478479	0.88[JPT][hapmap];0.84[ASN][1000 genomes]
rs10478481	0.96[ASN][1000 genomes]
rs10519639	0.85[CHB][hapmap];0.89[JPT][hapmap];0.95[ASN][1000 genomes]
rs10519640	0.85[CHB][hapmap];0.89[JPT][hapmap];0.95[ASN][1000 genomes]
rs11750856	0.88[JPT][hapmap]
rs12109575	0.88[JPT][hapmap]
rs1404304	0.88[JPT][hapmap]
rs1524571	0.85[CHB][hapmap];0.89[JPT][hapmap];0.94[ASN][1000 genomes]
rs1524577	0.88[JPT][hapmap]
rs1608668	0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs1608669	0.82[AFR][1000 genomes]
rs300962	1.00[CEU][hapmap];0.88[JPT][hapmap];0.86[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs300965	0.93[AFR][1000 genomes]
rs300969	0.92[YRI][hapmap];0.93[AFR][1000 genomes]
rs55647516	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6883663	0.88[JPT][hapmap]
rs724896	0.91[JPT][hapmap];0.98[ASN][1000 genomes]
rs73786521	0.95[ASN][1000 genomes]
rs7442772	0.88[JPT][hapmap]
rs7710645	0.90[JPT][hapmap]
rs7711004	0.90[JPT][hapmap]
rs7712650	0.90[JPT][hapmap]
rs7728478	0.90[JPT][hapmap]
rs897309	0.86[JPT][hapmap]
rs9327149	0.90[JPT][hapmap]
rs9327150	0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs9885295	0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532200	chr5:119317901-120102513	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv830463	chr5:119806643-119968825	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv462427	chr5:119838923-119928674	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv599601	chr5:119838923-119928674	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1031453	chr5:119843593-120393038	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv948613	chr5:119861955-119999008	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv599602	chr5:119866504-120023393	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv949499	chr5:119869763-119999008	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv882787	chr5:119874306-119925692	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	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	chr5:119904800-119913200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:119904800-119931200	Weak transcription	Osteobl	bone
3	chr5:119905000-119925800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:119905600-119934600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr5:119907800-119934800	Weak transcription	HSMM	muscle
6	chr5:119908000-119919400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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