Variant report

Variant	rs7043298
Chromosome Location	chr9:16651521-16651522
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1003069	0.87[YRI][hapmap]
rs1029015	0.84[CHB][hapmap];0.84[ASN][1000 genomes]
rs10756772	0.85[ASN][1000 genomes]
rs10756773	0.83[ASN][1000 genomes]
rs10810579	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.85[ASN][1000 genomes]
rs10810580	0.83[YRI][hapmap]
rs10962519	0.91[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10962520	0.88[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11790341	0.92[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13290470	0.84[MEX][hapmap]
rs1415471	0.84[CHB][hapmap];0.88[CHD][hapmap];0.86[ASN][1000 genomes]
rs1890074	0.84[CHB][hapmap];0.84[CHD][hapmap];0.84[JPT][hapmap]
rs2050617	0.90[CHB][hapmap]
rs2275256	0.88[CEU][hapmap];0.86[CHD][hapmap];0.94[JPT][hapmap];0.80[MEX][hapmap];0.84[TSI][hapmap];0.83[YRI][hapmap];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4961727	0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs4961728	0.90[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs7019299	0.88[CEU][hapmap];0.90[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7033512	0.88[CEU][hapmap];0.90[CHB][hapmap];0.83[JPT][hapmap];0.81[MEX][hapmap];0.81[TSI][hapmap];0.87[YRI][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7034582	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs7046245	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9886876	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 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
7	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
8	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

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16629600-16653600	Weak transcription	HUVEC	blood vessel
2	chr9:16637800-16652600	Weak transcription	Fetal Stomach	stomach
3	chr9:16640000-16670800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:16643000-16651800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:16643200-16652600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr9:16643200-16652600	Weak transcription	NHLF	lung
7	chr9:16643200-16653400	Weak transcription	NHDF-Ad	bronchial
8	chr9:16643400-16652400	Weak transcription	Osteobl	bone
9	chr9:16643600-16653600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr9:16645000-16652600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr9:16646200-16652600	Weak transcription	Ovary	ovary
12	chr9:16646200-16656800	Weak transcription	HSMMtube	muscle
13	chr9:16646400-16656600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr9:16646600-16652000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr9:16646600-16652400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr9:16646600-16661000	Weak transcription	HSMM	muscle
17	chr9:16647200-16653600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr9:16649200-16656000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr9:16649400-16654200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr9:16650800-16652600	Enhancers	Rectal Smooth Muscle	rectum
21	chr9:16650800-16657600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr9:16651000-16652600	Enhancers	Colon Smooth Muscle	Colon
23	chr9:16651000-16652600	Enhancers	Fetal Lung	lung
24	chr9:16651200-16653400	Enhancers	Fetal Kidney	kidney
25	chr9:16651200-16656800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr9:16651400-16651600	Enhancers	Fetal Intestine Small	intestine
27	chr9:16651400-16651800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr9:16651400-16652200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:16651400-16653400	Enhancers	A549	lung
30	chr9:16651400-16653800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr9:16651400-16656800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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