Variant report

Variant	rs7852214
Chromosome Location	chr9:72532067-72532068
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10746756	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10780700	0.92[ASN][1000 genomes]
rs10780701	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10780702	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10780703	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10868262	0.85[ASN][1000 genomes]
rs10868308	0.83[ASN][1000 genomes]
rs10868315	0.83[ASN][1000 genomes]
rs10868316	0.83[ASN][1000 genomes]
rs11788737	0.82[ASN][1000 genomes]
rs12684384	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs13291959	0.95[ASN][1000 genomes]
rs1565688	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050920	chr9:72345297-72579301	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv893438	chr9:72363992-72720438	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv831612	chr9:72473778-72634253	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv893439	chr9:72500956-72568962	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1043276	chr9:72522231-72571726	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	1 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	chr9:72514000-72539600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:72520600-72535200	Weak transcription	HSMM	muscle
3	chr9:72531200-72532200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:72531200-72533800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:72531400-72532200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr9:72531400-72533600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr9:72531400-72533600	Enhancers	NHDF-Ad	bronchial
8	chr9:72531600-72532600	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr9:72531600-72533000	Enhancers	NHEK	skin
10	chr9:72531600-72533600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr9:72531600-72533600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:72531600-72533600	Enhancers	HMEC	breast
13	chr9:72531800-72532200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr9:72531800-72532200	Enhancers	HUVEC	blood vessel
15	chr9:72531800-72533400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:72531800-72533600	Enhancers	Osteobl	bone
17	chr9:72532000-72532600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:72532000-72533400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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