Variant report

Variant	rs288112
Chromosome Location	chr2:141510641-141510642
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10177120	0.82[CEU][hapmap]
rs10201280	0.83[CEU][hapmap]
rs10203227	0.91[CEU][hapmap]
rs10439180	0.82[CEU][hapmap]
rs12466110	1.00[CEU][hapmap]
rs12624056	0.91[CEU][hapmap]
rs13419407	0.91[CEU][hapmap]
rs1372255	0.91[CEU][hapmap]
rs1441452	0.84[CEU][hapmap]
rs1441455	0.91[CEU][hapmap]
rs1441456	0.85[CEU][hapmap]
rs1441458	0.88[CEU][hapmap]
rs1441459	1.00[CEU][hapmap]
rs1441460	0.95[CEU][hapmap]
rs167011	0.90[CEU][hapmap];0.93[ASN][1000 genomes]
rs169638	0.82[CEU][hapmap];0.92[ASN][1000 genomes]
rs185959	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2046507	0.92[CEU][hapmap]
rs208359	0.86[CEU][hapmap];0.94[ASN][1000 genomes]
rs2119610	1.00[CEU][hapmap]
rs2165506	0.81[CEU][hapmap]
rs2218241	0.80[ASN][1000 genomes]
rs2218242	1.00[CEU][hapmap]
rs288105	0.87[CEU][hapmap]
rs288108	0.89[ASN][1000 genomes]
rs288110	0.92[CEU][hapmap]
rs288111	0.87[CEU][hapmap];0.94[ASN][1000 genomes]
rs382721	1.00[CEU][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs387927	1.00[CEU][hapmap];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs414023	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs421523	0.92[ASN][1000 genomes]
rs4954852	0.92[CEU][hapmap]
rs655405	0.83[CEU][hapmap]
rs726340	0.92[CEU][hapmap]
rs7596671	1.00[CEU][hapmap]
rs9287299	0.82[CEU][hapmap]
rs989308	0.83[CEU][hapmap]
rs9967729	0.86[CEU][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	nsv875195	chr2:141407101-141542081	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv875198	chr2:141409166-141571329	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv875199	chr2:141409166-141600366	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv875201	chr2:141448312-141561255	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv875202	chr2:141448312-141587228	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv875203	chr2:141448312-141592252	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv875204	chr2:141496596-141592252	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv875205	chr2:141500692-141592252	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv875206	chr2:141504719-141571329	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141509200-141511200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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