Variant report

Variant	rs1535845
Chromosome Location	chr9:79038235-79038236
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10114264	0.85[EUR][1000 genomes]
rs10121699	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10124695	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10735646	0.82[EUR][1000 genomes]
rs10781362	0.83[ASN][1000 genomes]
rs10869767	0.84[ASN][1000 genomes]
rs10869773	0.87[ASN][1000 genomes]
rs10869780	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11144864	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs11144865	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs11144871	0.82[ASN][1000 genomes]
rs11144880	0.86[ASN][1000 genomes]
rs11144899	0.83[ASN][1000 genomes]
rs11144945	1.00[YRI][hapmap]
rs11788095	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12057052	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13288968	0.88[ASN][1000 genomes]
rs13295433	0.87[ASN][1000 genomes]
rs1961995	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2002423	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2251604	0.82[ASN][1000 genomes]
rs2377639	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs2490572	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2490574	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2490576	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2490579	0.82[ASN][1000 genomes]
rs2490583	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2490584	0.90[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2490586	1.00[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2501920	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2501922	0.81[ASN][1000 genomes]
rs2501923	0.82[ASN][1000 genomes]
rs2501925	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs2501927	0.82[ASN][1000 genomes]
rs2501928	0.80[ASN][1000 genomes]
rs2501930	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2501932	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2501937	0.87[ASN][1000 genomes]
rs2501938	0.87[ASN][1000 genomes]
rs2501939	0.87[ASN][1000 genomes]
rs2501940	0.83[EUR][1000 genomes]
rs2501942	0.84[EUR][1000 genomes]
rs3739729	0.82[ASN][1000 genomes]
rs4372070	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4745541	0.81[ASN][1000 genomes]
rs4745544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4745545	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4745546	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4745548	0.83[ASN][1000 genomes]
rs638410	1.00[YRI][hapmap]
rs6560517	0.87[ASN][1000 genomes]
rs6560519	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6560520	0.84[ASN][1000 genomes]
rs6560521	0.84[ASN][1000 genomes]
rs6560522	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs7847608	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7849239	0.87[ASN][1000 genomes]
rs7861089	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869152	chr9:78742197-79583399	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv931033	chr9:78850330-79366454	Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv893478	chr9:78933874-79101006	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv893479	chr9:78971253-79275226	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	esv3451027	chr9:79021447-79056132	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:79034800-79046000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:79035000-79038800	Weak transcription	Stomach Mucosa	stomach
3	chr9:79036800-79039200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr9:79037400-79039400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr9:79038000-79038400	Enhancers	Ovary	ovary
6	chr9:79038000-79038400	Flanking Active TSS	HepG2	liver
7	chr9:79038000-79038600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr9:79038000-79046800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:79038200-79039400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr9:79038200-79039600	Enhancers	Primary T cells from cord blood	blood
11	chr9:79038200-79039800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links