Variant report

Variant	rs10981026
Chromosome Location	chr9:99951497-99951498
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10114464	1.00[CEU][hapmap]
rs10116686	1.00[CEU][hapmap]
rs10121540	1.00[CEU][hapmap]
rs10817175	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10817176	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10817177	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10817178	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10817179	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10817180	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10817181	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10817183	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10817192	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10817211	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10817263	0.81[EUR][1000 genomes]
rs10817266	1.00[CEU][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs10817369	1.00[CEU][hapmap]
rs10817378	0.93[TSI][hapmap]
rs10980872	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10980873	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10980889	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10980894	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10980896	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10980912	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10980939	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10981015	0.84[ASN][1000 genomes]
rs10981062	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs10981130	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981301	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs10981569	1.00[CEU][hapmap]
rs11789331	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11792076	0.99[EUR][1000 genomes]
rs11792723	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11792736	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11794757	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11795173	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12235225	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12235677	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12237438	0.91[EUR][1000 genomes]
rs12237510	0.81[EUR][1000 genomes]
rs12237712	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12237849	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12238318	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12238745	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12686392	0.81[EUR][1000 genomes]
rs1986463	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35085150	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3747502	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs3747509	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs3953684	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs41281914	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4263876	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4436243	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs56722769	0.89[EUR][1000 genomes]
rs57176573	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57936136	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58723976	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61050463	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7025132	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs7032137	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73654680	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73654686	0.81[EUR][1000 genomes]
rs73654687	0.80[EUR][1000 genomes]
rs7849583	0.88[AMR][1000 genomes]
rs7855042	1.00[CEU][hapmap]
rs7858368	1.00[CEU][hapmap]

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	nsv972432	chr9:99874607-99958095	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv931946	chr9:99895658-100005099	Bivalent/Poised TSS Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv893607	chr9:99906545-99996548	Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv893608	chr9:99906545-100005128	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99911600-99957600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:99934400-99951600	Strong transcription	H1 Cell Line	embryonic stem cell
3	chr9:99934400-99957800	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr9:99934800-99957400	Strong transcription	HUES64 Cell Line	embryonic stem cell
5	chr9:99936400-99953200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
6	chr9:99936600-99957600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
7	chr9:99936800-99951800	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr9:99942800-99962600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr9:99947200-99951600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
10	chr9:99949200-99962400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr9:99951200-99954800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:99951200-99955400	Weak transcription	H9 Cell Line	embryonic stem cell

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