Variant report

Variant	rs1003070
Chromosome Location	chr9:16640682-16640683
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1003069	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10810579	0.81[EUR][1000 genomes]
rs10810580	0.93[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs10810581	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1337390	0.81[ASN][1000 genomes]
rs4131372	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4961728	0.90[EUR][1000 genomes]
rs7034582	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7039706	0.82[ASN][1000 genomes]
rs958557	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9886876	0.82[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	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
6	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

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16629200-16642200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr9:16629600-16653600	Weak transcription	HUVEC	blood vessel
3	chr9:16630000-16642400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr9:16636000-16641800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr9:16636000-16642000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:16636400-16642400	Weak transcription	NHDF-Ad	bronchial
7	chr9:16636400-16645800	Weak transcription	Ovary	ovary
8	chr9:16637800-16644600	Weak transcription	Fetal Lung	lung
9	chr9:16637800-16652600	Weak transcription	Fetal Stomach	stomach
10	chr9:16638000-16651200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr9:16638200-16640800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr9:16638200-16644600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr9:16638400-16640800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr9:16638400-16642600	Weak transcription	Osteobl	bone
15	chr9:16638400-16644800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr9:16639000-16640800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:16640000-16670800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:16640200-16641000	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr9:16640200-16641400	Enhancers	A549	lung
20	chr9:16640400-16641400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr9:16640400-16641400	Enhancers	Colon Smooth Muscle	Colon
22	chr9:16640400-16641600	Enhancers	HSMM	muscle
23	chr9:16640600-16640800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr9:16640600-16641000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr9:16640600-16641000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr9:16640600-16641000	Enhancers	Rectal Smooth Muscle	rectum
27	chr9:16640600-16641000	Enhancers	HSMMtube	muscle
28	chr9:16640600-16641200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr9:16640600-16641200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr9:16640600-16641200	Enhancers	Fetal Kidney	kidney
31	chr9:16640600-16641200	Enhancers	NHLF	lung
32	chr9:16640600-16643400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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