Variant report

Variant	rs3927535
Chromosome Location	chr9:16787528-16787529
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10733321	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10810618	1.00[JPT][hapmap];0.82[TSI][hapmap]
rs10810623	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13289196	1.00[CEU][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.94[TSI][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1330300	1.00[JPT][hapmap];0.87[YRI][hapmap]
rs1330301	0.87[CEU][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1537002	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2026803	1.00[ASN][1000 genomes]
rs2243614	1.00[JPT][hapmap];0.91[MEX][hapmap]
rs2243836	1.00[ASN][1000 genomes]
rs2254193	1.00[JPT][hapmap];0.91[MEX][hapmap]
rs2254468	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs2480924	1.00[ASN][1000 genomes]
rs4961495	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4961756	1.00[ASN][1000 genomes]
rs4961759	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4961760	0.82[MEX][hapmap]
rs6475071	1.00[JPT][hapmap]
rs6475079	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6475081	1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.89[TSI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7037653	1.00[JPT][hapmap];0.85[YRI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7850168	1.00[ASW][hapmap];0.87[CEU][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs7859111	0.87[CEU][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7860932	1.00[CEU][hapmap];0.89[GIH][hapmap];0.91[MEX][hapmap];0.89[TSI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7873181	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9407777	1.00[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	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	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription 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	20 gene(s)	inside rSNPs	diseases
3	esv2758627	chr9:16641966-16809203	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2759673	chr9:16641966-16809203	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription 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	10 gene(s)	inside rSNPs	diseases
5	nsv892650	chr9:16696187-16950860	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16767600-16795400	Weak transcription	Fetal Muscle Leg	muscle
2	chr9:16768000-16795000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:16769800-16787600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:16769800-16795400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:16773000-16795000	Weak transcription	HSMMtube	muscle
6	chr9:16776000-16787600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr9:16784400-16802200	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr9:16785000-16792200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr9:16785200-16794600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:16786000-16787600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:16786000-16795600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr9:16786600-16788000	Strong transcription	Fetal Stomach	stomach
13	chr9:16786600-16788200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:16786800-16787600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr9:16786800-16787600	Strong transcription	NHLF	lung
16	chr9:16787000-16787600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr9:16787000-16788000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr9:16787000-16788200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr9:16787000-16792400	Weak transcription	Colon Smooth Muscle	Colon
20	chr9:16787000-16794600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr9:16787000-16795200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr9:16787200-16787800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:16787200-16788200	Enhancers	NHDF-Ad	bronchial
24	chr9:16787200-16794800	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr9:16787200-16797600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:16787400-16787600	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr9:16787400-16787600	Genic enhancers	Stomach Smooth Muscle	stomach
28	chr9:16787400-16788000	Enhancers	NH-A	brain
29	chr9:16787400-16788200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr9:16787400-16788200	Genic enhancers	HSMM	muscle
31	chr9:16787400-16788200	Enhancers	HUVEC	blood vessel
32	chr9:16787400-16788200	Enhancers	Osteobl	bone
33	chr9:16787400-16788400	Strong transcription	Ovary	ovary

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