Variant report

Variant	rs2039584
Chromosome Location	chr9:21676295-21676296
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11999970	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13287072	0.84[ASN][1000 genomes]
rs1478058	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16938532	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16938533	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1869205	0.82[CHB][hapmap];0.80[JPT][hapmap]
rs2020334	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2020344	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2039585	0.81[ASN][1000 genomes]
rs2083560	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2383200	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2383201	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2891163	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4307419	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6475544	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6475546	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7021741	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7028436	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7028637	0.84[ASN][1000 genomes]
rs7028950	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7029077	0.84[ASN][1000 genomes]
rs7035252	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7035284	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7852691	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7860632	0.84[ASN][1000 genomes]
rs7865123	0.87[CHB][hapmap];0.80[ASN][1000 genomes]
rs7865502	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7866337	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7866521	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs921560	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029634	chr9:21542970-21765286	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv1015623	chr9:21579110-21694039	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
3	nsv892742	chr9:21589041-21707372	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv892743	chr9:21675545-21772064	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21673000-21679400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr9:21674200-21677600	Enhancers	HMEC	breast
3	chr9:21674200-21678200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:21674400-21677600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:21674600-21676600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr9:21674600-21677400	Enhancers	NHEK	skin
7	chr9:21674600-21677600	Enhancers	NHDF-Ad	bronchial
8	chr9:21674800-21676800	Enhancers	Hela-S3	cervix
9	chr9:21674800-21677400	Enhancers	HUVEC	blood vessel
10	chr9:21674800-21677600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr9:21675000-21676400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr9:21675000-21677400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr9:21675000-21677600	Enhancers	Osteobl	bone
14	chr9:21675400-21676600	Enhancers	NHLF	lung
15	chr9:21675400-21676800	Flanking Active TSS	A549	lung
16	chr9:21675600-21677600	Weak transcription	NH-A	brain
17	chr9:21675800-21677600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:21676200-21678600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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