Variant report

Variant	rs72755718
Chromosome Location	chr5:57521909-57521910
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:32)

rs_ID	r²[population]
rs1035473	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10513135	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11737991	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11738845	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11740290	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11744441	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11745219	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11746013	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11747017	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11749817	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11750320	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12515401	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs17696079	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs17764094	0.88[ASN][1000 genomes]
rs1971059	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1971060	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2409007	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4700259	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4700268	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4700269	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4700273	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs66884124	0.87[ASN][1000 genomes]
rs72755724	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72755726	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72755728	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72755729	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72755745	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs72755750	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs72755767	0.88[ASN][1000 genomes]
rs7701350	0.87[ASN][1000 genomes]
rs7733184	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs969473	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432746	chr5:57502859-57547419	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57520600-57526000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr5:57520800-57526000	Weak transcription	NHEK	skin
3	chr5:57521000-57522000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr5:57521000-57526000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:57521200-57522200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:57521200-57522200	Weak transcription	Adipose Nuclei	Adipose
7	chr5:57521200-57522200	Weak transcription	Osteobl	bone
8	chr5:57521600-57522200	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr5:57521800-57522000	Enhancers	Psoas Muscle	Psoas
10	chr5:57521800-57535600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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