Variant report

Variant	rs10116857
Chromosome Location	chr9:16595649-16595650
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10117448	1.00[CEU][hapmap]
rs10118895	0.80[EUR][1000 genomes]
rs10120281	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10121959	0.89[EUR][1000 genomes]
rs10122372	0.84[EUR][1000 genomes]
rs10123480	1.00[CEU][hapmap]
rs10123558	0.82[CEU][hapmap]
rs10124530	0.82[EUR][1000 genomes]
rs10511622	1.00[CEU][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs10733311	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10733312	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10738437	0.82[CEU][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10738439	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10738440	0.80[EUR][1000 genomes]
rs10756763	1.00[CEU][hapmap]
rs10756764	0.80[EUR][1000 genomes]
rs10810576	0.82[CEU][hapmap]
rs10962484	0.84[EUR][1000 genomes]
rs10962492	0.82[CEU][hapmap];0.86[EUR][1000 genomes]
rs10962493	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10962494	0.82[CEU][hapmap]
rs10962510	0.80[EUR][1000 genomes]
rs10962511	1.00[CEU][hapmap]
rs12000426	0.91[EUR][1000 genomes]
rs12002673	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs12004304	0.89[EUR][1000 genomes]
rs12337676	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12338548	1.00[CEU][hapmap]
rs12339625	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12340504	0.93[EUR][1000 genomes]
rs12343239	0.88[EUR][1000 genomes]
rs12343306	0.88[EUR][1000 genomes]
rs12350242	1.00[CEU][hapmap];0.83[YRI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12350853	0.82[CEU][hapmap]
rs12352543	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1337393	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1337400	1.00[CEU][hapmap];0.86[YRI][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1415473	0.94[EUR][1000 genomes]
rs1415474	1.00[CEU][hapmap];0.83[YRI][hapmap]
rs1415475	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1415476	1.00[CEU][hapmap];0.85[YRI][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1538102	0.82[EUR][1000 genomes]
rs16934816	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16934842	1.00[EUR][1000 genomes]
rs16934855	0.91[EUR][1000 genomes]
rs16934886	0.82[EUR][1000 genomes]
rs17738890	0.82[EUR][1000 genomes]
rs1927616	1.00[CEU][hapmap]
rs1927617	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs1927618	0.82[CEU][hapmap]
rs1927626	1.00[CEU][hapmap];0.86[YRI][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1952345	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs1952346	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2065937	0.91[EUR][1000 genomes]
rs2095657	0.91[EUR][1000 genomes]
rs2149159	0.85[EUR][1000 genomes]
rs2382808	1.00[CEU][hapmap]
rs2382809	1.00[CEU][hapmap]
rs2382810	1.00[CEU][hapmap]
rs28428651	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28457730	0.82[AMR][1000 genomes]
rs28490464	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28501274	0.89[EUR][1000 genomes]
rs28648047	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28651010	0.86[EUR][1000 genomes]
rs28733737	0.94[EUR][1000 genomes]
rs2891072	1.00[CEU][hapmap]
rs4466493	0.82[EUR][1000 genomes]
rs4961725	0.85[EUR][1000 genomes]
rs56218971	0.82[EUR][1000 genomes]
rs6475059	1.00[CEU][hapmap]
rs6475060	1.00[CEU][hapmap]
rs6475062	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs6475063	0.88[EUR][1000 genomes]
rs7018743	0.87[EUR][1000 genomes]
rs7018877	0.85[EUR][1000 genomes]
rs7019016	0.85[EUR][1000 genomes]
rs7019105	0.85[EUR][1000 genomes]
rs7019625	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7032239	0.87[EUR][1000 genomes]
rs7032772	0.82[EUR][1000 genomes]
rs7036282	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7048399	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7048805	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs725011	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73417477	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7350234	1.00[CEU][hapmap]
rs7470623	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7850123	0.82[CEU][hapmap];0.86[EUR][1000 genomes]
rs7854979	0.85[EUR][1000 genomes]
rs7856477	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs7858025	0.82[CEU][hapmap]
rs7859395	0.86[EUR][1000 genomes]
rs7859971	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7863885	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs7870380	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs7870508	0.82[EUR][1000 genomes]
rs7870730	0.82[EUR][1000 genomes]
rs7873338	0.91[EUR][1000 genomes]
rs943745	1.00[CEU][hapmap]

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	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv530934	chr9:16281246-16779432	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1032856	chr9:16465330-16773471	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv540073	chr9:16465330-16773471	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16576000-16601600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:16576400-16601400	Weak transcription	NHDF-Ad	bronchial
3	chr9:16583000-16606800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:16583200-16611200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:16586000-16596000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr9:16586800-16604400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr9:16587400-16597200	Weak transcription	Fetal Stomach	stomach
8	chr9:16591400-16598600	Weak transcription	HSMM	muscle
9	chr9:16594200-16596000	Enhancers	Ovary	ovary
10	chr9:16594600-16596600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr9:16594800-16596400	Weak transcription	Colon Smooth Muscle	Colon
12	chr9:16594800-16596600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr9:16594800-16601800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr9:16594800-16601800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr9:16595000-16596600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr9:16595000-16596600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr9:16595000-16596600	Weak transcription	Fetal Lung	lung
18	chr9:16595000-16597200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr9:16595000-16598000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr9:16595000-16598000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:16595000-16611200	Weak transcription	NHLF	lung
22	chr9:16595200-16597600	Enhancers	A549	lung
23	chr9:16595200-16598400	Weak transcription	Osteobl	bone
24	chr9:16595400-16597600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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