Variant report

Variant	rs12341168
Chromosome Location	chr9:16793202-16793203
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10115109	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10119731	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10119811	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10120562	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10121347	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs10122827	0.86[CHB][hapmap]
rs10122901	0.88[EUR][1000 genomes]
rs10125996	1.00[CEU][hapmap];0.83[JPT][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10810622	0.90[CHB][hapmap]
rs10810635	0.87[YRI][hapmap];0.87[AFR][1000 genomes]
rs10962588	0.90[CHB][hapmap]
rs10962592	0.82[EUR][1000 genomes]
rs10962601	1.00[CEU][hapmap];0.83[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10962609	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs12338608	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12341542	0.85[AMR][1000 genomes]
rs12351269	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12376135	0.87[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs12378588	0.88[AMR][1000 genomes]
rs12378598	0.84[AMR][1000 genomes]
rs12380481	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16935073	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs2039185	0.90[CHB][hapmap]
rs2183406	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2183407	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2253579	0.88[CEU][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28584140	0.82[EUR][1000 genomes]
rs4455968	0.83[EUR][1000 genomes]
rs7024466	0.81[CHB][hapmap]
rs7861591	1.00[CEU][hapmap];0.81[CHB][hapmap];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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
6	nsv613671	chr9:16792350-16804082	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:28 , 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	chr9:16769800-16795400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:16773000-16795000	Weak transcription	HSMMtube	muscle
5	chr9:16784400-16802200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:16785200-16794600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr9:16786000-16795600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr9:16787000-16794600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr9:16787000-16795200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:16787200-16794800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr9:16787200-16797600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:16787600-16795000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr9:16788000-16795000	Weak transcription	Fetal Stomach	stomach
14	chr9:16788200-16794400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr9:16788200-16794600	Weak transcription	NHDF-Ad	bronchial
16	chr9:16788200-16794800	Weak transcription	HSMM	muscle
17	chr9:16788200-16795000	Weak transcription	NHLF	lung
18	chr9:16788200-16798000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr9:16789000-16794200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr9:16790400-16793800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr9:16792000-16794600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr9:16792200-16793600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:16792200-16793600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr9:16792200-16794000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr9:16792400-16796200	Enhancers	Colon Smooth Muscle	Colon
26	chr9:16792600-16793400	Weak transcription	Ovary	ovary
27	chr9:16792600-16794800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr9:16793000-16794600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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