Variant report

Variant	rs10908646
Chromosome Location	chr1:158292366-158292367
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10797006	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs10797008	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10908644	0.81[EUR][1000 genomes]
rs10908645	0.95[EUR][1000 genomes]
rs10908647	1.00[ASN][1000 genomes]
rs11264949	0.84[EUR][1000 genomes]
rs11264950	0.92[EUR][1000 genomes]
rs11264952	0.93[EUR][1000 genomes]
rs11486132	0.90[EUR][1000 genomes]
rs11488686	0.95[EUR][1000 genomes]
rs12027881	0.81[EUR][1000 genomes]
rs12038925	0.80[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12077077	0.83[EUR][1000 genomes]
rs12077284	0.80[EUR][1000 genomes]
rs12089293	0.83[EUR][1000 genomes]
rs12095313	0.93[EUR][1000 genomes]
rs12407446	0.81[EUR][1000 genomes]
rs12409817	0.83[EUR][1000 genomes]
rs1813777	0.86[EUR][1000 genomes]
rs1923141	0.91[EUR][1000 genomes]
rs2317883	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3176842	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3176843	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34591069	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35752748	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs366316	1.00[CEU][hapmap]
rs440710	0.80[EUR][1000 genomes]
rs4489554	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59038586	0.85[ASN][1000 genomes]
rs60706492	0.90[ASN][1000 genomes]
rs6685958	0.80[EUR][1000 genomes]
rs716221	0.80[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73029766	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7539343	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999542	chr1:158015715-158368132	Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv872479	chr1:158118787-158484285	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv872480	chr1:158153526-158450238	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv831692	chr1:158223459-158392016	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10908646	CD1A	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158290000-158293200	Weak transcription	Primary B cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links