Variant report

Variant	rs839128
Chromosome Location	chr12:86549655-86549656
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10858411	1.00[CHB][hapmap]
rs1097997	1.00[CHB][hapmap]
rs11117189	1.00[CHB][hapmap]
rs1389292	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1463750	1.00[CHB][hapmap]
rs1493414	1.00[CHB][hapmap]
rs1532263	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1689340	0.83[CEU][hapmap]
rs1689364	1.00[CHB][hapmap]
rs1698757	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs2452808	1.00[CHB][hapmap]
rs2471560	0.86[TSI][hapmap]
rs2471565	1.00[CHB][hapmap]
rs2897273	1.00[CHB][hapmap]
rs4265650	0.80[CEU][hapmap]
rs6538021	1.00[ASN][1000 genomes]
rs6538025	0.85[TSI][hapmap]
rs6538027	1.00[CHB][hapmap]
rs7134944	1.00[CHB][hapmap]
rs7312245	1.00[CHB][hapmap]
rs839094	1.00[ASN][1000 genomes]
rs839099	1.00[CHB][hapmap]
rs839100	1.00[CHB][hapmap]
rs839104	0.90[TSI][hapmap]
rs839105	0.86[TSI][hapmap]
rs839106	1.00[CHB][hapmap]
rs839107	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs839109	1.00[CHB][hapmap]
rs839112	1.00[ASN][1000 genomes]
rs839113	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839114	1.00[CHB][hapmap]
rs839115	1.00[CHB][hapmap]
rs839116	1.00[CHB][hapmap]
rs839118	1.00[CEU][hapmap]
rs839119	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs839120	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap]
rs839123	1.00[CEU][hapmap]
rs839124	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs839134	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs839137	0.88[CEU][hapmap]
rs839138	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs839139	1.00[CHB][hapmap]
rs839147	1.00[CHB][hapmap]
rs839157	0.90[TSI][hapmap]
rs839165	0.85[TSI][hapmap]
rs839171	0.90[TSI][hapmap]
rs839182	0.92[CEU][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs839183	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs839185	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839186	1.00[ASN][1000 genomes]
rs839188	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839189	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.84[MEX][hapmap];0.97[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839191	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs844435	0.90[TSI][hapmap]
rs844437	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs858213	1.00[CHB][hapmap]
rs863395	0.90[TSI][hapmap]
rs865722	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs866893	0.96[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2761759	chr12:86415936-86747726	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv518059	chr12:86416212-86747726	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041397	chr12:86438607-86737558	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv470311	chr12:86484366-86550783	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3442004	chr12:86514695-86599965	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv2753278	chr12:86522507-86555154	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv510606	chr12:86545449-86555302	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links