Variant report

Variant	rs73435650
Chromosome Location	chr9:21681118-21681119
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs16938530	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16938531	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16938541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16938544	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1953348	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435661	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435664	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[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:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21677200-21684600	Enhancers	Hela-S3	cervix
2	chr9:21678000-21683200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr9:21678000-21688200	Enhancers	HMEC	breast
4	chr9:21678200-21681600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:21678200-21681600	Enhancers	NHDF-Ad	bronchial
6	chr9:21678200-21681800	Enhancers	NHEK	skin
7	chr9:21678200-21684000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:21678400-21687400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:21678600-21681600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr9:21678600-21684600	Enhancers	HUVEC	blood vessel
11	chr9:21679400-21681600	Weak transcription	Stomach Mucosa	stomach
12	chr9:21679800-21682600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:21680400-21681200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr9:21680400-21681600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr9:21680400-21683400	Enhancers	HSMM	muscle
16	chr9:21680400-21684200	Enhancers	NHLF	lung
17	chr9:21680400-21684600	Enhancers	NH-A	brain
18	chr9:21680400-21685000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr9:21680400-21686000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr9:21680400-21688200	Flanking Active TSS	A549	lung
21	chr9:21680400-21688200	Enhancers	Osteobl	bone
22	chr9:21680400-21691000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr9:21680600-21681600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr9:21681000-21681200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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