Variant report

Variant	rs17185631
Chromosome Location	chr9:17948869-17948870
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10963347	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10963348	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10963360	0.89[EUR][1000 genomes]
rs11788965	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11793268	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12006255	0.82[EUR][1000 genomes]
rs12115754	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12552709	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16936157	0.90[EUR][1000 genomes]
rs17186224	0.89[EUR][1000 genomes]
rs1778167	0.86[EUR][1000 genomes]
rs1778180	0.84[EUR][1000 genomes]
rs2026766	0.89[EUR][1000 genomes]
rs2026767	0.90[EUR][1000 genomes]
rs4517213	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs55712364	0.90[EUR][1000 genomes]
rs56310081	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56315315	0.90[EUR][1000 genomes]
rs7029738	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72695939	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72695951	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72695987	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7866746	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs884097	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv613706	chr9:17718918-18090934	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv613707	chr9:17720175-18070475	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv613708	chr9:17720175-18072085	Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv1795741	chr9:17880109-17951331	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	esv1797946	chr9:17880109-17951331	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
6	esv1818676	chr9:17880109-17951331	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
7	esv1829631	chr9:17880109-17951331	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
8	esv1830694	chr9:17880109-17951331	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
9	esv1834674	chr9:17880109-17951331	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
10	esv1836647	chr9:17880109-17951331	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
11	esv1845722	chr9:17880109-17951331	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
12	esv1849548	chr9:17880109-17951331	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
13	nsv892676	chr9:17911466-17987408	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
14	nsv892677	chr9:17918806-18002205	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	inside rSNPs	diseases
15	nsv1020855	chr9:17929044-17975791	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
16	nsv1021862	chr9:17931213-18052101	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17940200-17962200	Weak transcription	Aorta	Aorta
2	chr9:17947600-17949400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr9:17948200-17949000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr9:17948200-17949000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr9:17948200-17949600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr9:17948200-17949800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr9:17948400-17949600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr9:17948800-17950000	Enhancers	Fetal Heart	heart

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