Variant report

Variant	rs10980873
Chromosome Location	chr9:99913624-99913625
allele	C/T
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:63)

rs_ID	r²[population]
rs10114464	0.87[CEU][hapmap]
rs10116686	0.87[CEU][hapmap]
rs10121540	0.87[CEU][hapmap]
rs10817175	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10817176	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10817177	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10817178	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10817179	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10817180	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10817181	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10817183	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10817192	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10817211	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10817263	0.82[EUR][1000 genomes]
rs10817266	0.87[CEU][hapmap];0.93[TSI][hapmap];0.80[EUR][1000 genomes]
rs10817369	0.85[CEU][hapmap]
rs10817378	0.87[TSI][hapmap]
rs10980872	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10980889	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10980894	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10980896	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10980912	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10980939	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10981026	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10981062	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs10981130	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10981301	0.87[CEU][hapmap];0.82[EUR][1000 genomes]
rs10981569	0.87[CEU][hapmap]
rs11789331	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11792076	0.99[EUR][1000 genomes]
rs11792723	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11792736	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11794757	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11795173	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12235225	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12235677	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12237438	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12237510	0.82[EUR][1000 genomes]
rs12237712	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12237849	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12238318	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12238745	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12686392	0.82[EUR][1000 genomes]
rs1986463	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35085150	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3747502	0.87[CEU][hapmap];0.93[TSI][hapmap]
rs3747509	0.87[CEU][hapmap];0.93[TSI][hapmap]
rs3953684	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41281914	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4263876	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4436243	0.87[CEU][hapmap];0.93[TSI][hapmap]
rs56722769	0.86[EUR][1000 genomes]
rs57176573	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57936136	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58723976	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61050463	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7025132	0.87[CEU][hapmap];0.93[TSI][hapmap]
rs7032137	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73654680	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73654686	0.82[EUR][1000 genomes]
rs73654687	0.80[EUR][1000 genomes]
rs7855042	0.87[CEU][hapmap]
rs7858368	0.87[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831662	chr9:99752521-99939231	Bivalent Enhancer Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	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
3	nsv973382	chr9:99894731-99916071	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	inside rSNPs	diseases
4	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
5	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
6	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:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99901000-99921000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:99909800-99920200	Weak transcription	Brain Angular Gyrus	brain
3	chr9:99911600-99957600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr9:99912200-99915200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:99912200-99915400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:99912200-99921200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:99912200-99922800	Weak transcription	Brain Anterior Caudate	brain
8	chr9:99912200-99923800	Strong transcription	H1 Cell Line	embryonic stem cell
9	chr9:99912800-99915000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
10	chr9:99913000-99920000	Strong transcription	H9 Cell Line	embryonic stem cell
11	chr9:99913000-99924400	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:99913200-99923600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
13	chr9:99913200-99924200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:99913400-99918400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr9:99913400-99924600	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr9:99913400-99930800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
17	chr9:99913600-99914800	Weak transcription	Fetal Intestine Small	intestine
18	chr9:99913600-99924200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
19	chr9:99913600-99930800	Strong transcription	HUES64 Cell Line	embryonic stem cell

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