Variant report

Variant	rs9837419
Chromosome Location	chr3:157501344-157501345
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10222405	0.95[ASN][1000 genomes]
rs10446283	0.95[ASN][1000 genomes]
rs10446335	0.95[ASN][1000 genomes]
rs10936108	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11709138	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11712832	0.95[ASN][1000 genomes]
rs1552486	0.95[ASN][1000 genomes]
rs1552487	0.95[ASN][1000 genomes]
rs1685680	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1979577	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1994480	0.95[ASN][1000 genomes]
rs2054863	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2054864	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3845979	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7630713	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs792738	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs792739	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs792740	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs807201	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs809395	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs901820	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9809803	0.95[ASN][1000 genomes]
rs9816230	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9833772	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9836369	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9847213	0.95[ASN][1000 genomes]
rs9857956	0.97[ASN][1000 genomes]
rs9867271	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9876088	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9882048	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv592121	chr3:157437068-157593470	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv997770	chr3:157441619-157595315	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3388089	chr3:157499858-157501806	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157500400-157502200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr3:157500400-157502200	Weak transcription	Osteobl	bone
3	chr3:157500400-157502600	Weak transcription	NHLF	lung
4	chr3:157500600-157501600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr3:157500600-157501600	Weak transcription	NHDF-Ad	bronchial
6	chr3:157501200-157501600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr3:157501200-157501600	Weak transcription	Aorta	Aorta

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