Variant report

Variant	rs1891043
Chromosome Location	chr9:18575676-18575677
allele	C/T
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:28)

rs_ID	r²[population]
rs10119114	1.00[CEU][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10511637	1.00[CEU][hapmap]
rs1147795	1.00[CEU][hapmap]
rs11794207	0.81[ASN][1000 genomes]
rs12001288	1.00[CEU][hapmap]
rs1341057	0.90[ASN][1000 genomes]
rs1361533	1.00[CEU][hapmap]
rs16936777	1.00[CEU][hapmap]
rs16936819	1.00[CHB][hapmap]
rs16936827	0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs16936853	1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[ASN][1000 genomes]
rs1856893	0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs1891042	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2383077	0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs55686384	0.84[ASN][1000 genomes]
rs57339828	0.84[ASN][1000 genomes]
rs58417061	0.84[ASN][1000 genomes]
rs58504170	0.97[ASN][1000 genomes]
rs59401514	0.87[ASN][1000 genomes]
rs60498809	0.84[ASN][1000 genomes]
rs61210955	0.87[ASN][1000 genomes]
rs61364591	0.84[ASN][1000 genomes]
rs7031043	0.87[ASN][1000 genomes]
rs7044968	1.00[CEU][hapmap]
rs73644234	0.87[ASN][1000 genomes]
rs7469307	0.81[ASN][1000 genomes]
rs7871056	0.87[ASN][1000 genomes]
rs9775632	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1029449	chr9:18414752-18829127	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv540077	chr9:18414752-18829127	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1030931	chr9:18414752-18903530	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv892690	chr9:18485434-18592374	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
8	nsv428536	chr9:18512807-18667760	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
9	nsv892691	chr9:18519699-18805483	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv892692	chr9:18519699-19045502	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv892693	chr9:18541710-18584860	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
12	esv2430566	chr9:18574479-18575902	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18564400-18591800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:18566800-18579600	Weak transcription	HSMMtube	muscle
3	chr9:18567000-18579600	Weak transcription	HUVEC	blood vessel
4	chr9:18567800-18578000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:18569600-18580200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:18569800-18601000	Weak transcription	NHLF	lung
7	chr9:18570200-18583200	Weak transcription	Fetal Stomach	stomach
8	chr9:18570200-18591800	Weak transcription	Aorta	Aorta
9	chr9:18571800-18579200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:18573200-18579000	Strong transcription	HSMM	muscle
11	chr9:18574400-18581600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:18574600-18576200	Weak transcription	Osteobl	bone
13	chr9:18575000-18581000	Weak transcription	NHDF-Ad	bronchial
14	chr9:18575400-18576000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr9:18575400-18576400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr9:18575400-18581600	Weak transcription	NH-A	brain
17	chr9:18575600-18576000	Genic enhancers	Muscle Satellite Cultured Cells	--
18	chr9:18575600-18576200	Enhancers	Pancreatic Islets	Pancreatic Islet

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