Variant report

Variant	rs7049170
Chromosome Location	chr9:16610456-16610457
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10118895	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10120281	0.90[ASN][1000 genomes]
rs10122372	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10125014	1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10733311	0.90[ASN][1000 genomes]
rs10738437	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10738440	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10738441	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10738442	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10738443	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10756764	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10756765	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10756766	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10756767	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10756768	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10756770	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10756774	0.93[AMR][1000 genomes]
rs10756775	0.93[AMR][1000 genomes]
rs10962510	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12004304	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12350242	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1415474	1.00[JPT][hapmap]
rs1538102	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs16934816	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16934842	0.88[AMR][1000 genomes]
rs16934855	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16934875	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16934886	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17738890	0.88[AMR][1000 genomes]
rs2095657	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2149159	0.83[AMR][1000 genomes]
rs28490464	0.90[ASN][1000 genomes]
rs28501274	0.90[ASN][1000 genomes]
rs28651010	0.90[ASN][1000 genomes]
rs34950291	0.90[ASN][1000 genomes]
rs4466493	0.90[ASN][1000 genomes]
rs4961725	0.82[EUR][1000 genomes]
rs4961726	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7018743	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7018877	1.00[JPT][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7019016	1.00[JPT][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7019105	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7032239	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7032772	0.84[EUR][1000 genomes]
rs7034606	0.89[EUR][1000 genomes]
rs7035303	0.89[EUR][1000 genomes]
rs7049082	0.84[EUR][1000 genomes]
rs73421425	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7470623	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7854979	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7859395	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7870508	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7870730	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7873338	0.90[ASN][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	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
5	nsv524264	chr9:16596071-16611692	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv430000	chr9:16603483-16671045	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16583200-16611200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr9:16595000-16611200	Weak transcription	NHLF	lung
3	chr9:16597600-16610800	Weak transcription	Fetal Stomach	stomach
4	chr9:16598800-16611400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:16599000-16612200	Weak transcription	Osteobl	bone
6	chr9:16599000-16612600	Weak transcription	HSMM	muscle
7	chr9:16602800-16612400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:16603200-16612600	Weak transcription	HUVEC	blood vessel
9	chr9:16606200-16613600	Weak transcription	HSMMtube	muscle
10	chr9:16606200-16615000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr9:16607000-16618400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:16608200-16610800	Weak transcription	Colon Smooth Muscle	Colon
13	chr9:16608400-16618600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr9:16608800-16610800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr9:16609400-16612200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr9:16609400-16613600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr9:16609600-16611400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr9:16609600-16611400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr9:16609600-16612600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr9:16609600-16618000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr9:16609600-16619800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr9:16610000-16611000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr9:16610000-16611400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr9:16610000-16612800	Weak transcription	Ovary	ovary
25	chr9:16610200-16611200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr9:16610200-16611400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr9:16610200-16614400	Enhancers	NHDF-Ad	bronchial

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