Variant report

Variant	rs10981158
Chromosome Location	chr9:99973318-99973319
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10521028	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10980890	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10980955	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10980992	0.82[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs10981005	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10981161	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10981297	0.85[AFR][1000 genomes]
rs12377244	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12378555	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12550862	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12555636	0.81[AMR][1000 genomes]
rs13286601	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13287095	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16905669	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1857085	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1986462	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34592472	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34868501	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35241252	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35285539	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4014782	0.82[EUR][1000 genomes]
rs4128763	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4463540	0.85[EUR][1000 genomes]
rs4743061	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4743062	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56860287	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs58003970	0.87[EUR][1000 genomes]
rs7018753	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7021506	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7848439	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7851025	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7860303	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7865758	0.87[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	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
2	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
3	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
4	nsv972433	chr9:99962059-99983443	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10981158	VN1R51P	cis	Thyroid	GTEx

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99968200-99973400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:99968200-99975200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:99968200-99976800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:99968200-99976800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:99968800-99973600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr9:99968800-99973600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr9:99969000-99973600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr9:99969000-99973600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr9:99972400-99973400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr9:99973200-99973600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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