Variant report

Variant	rs2219975
Chromosome Location	chr3:99070019-99070020
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:28)

rs_ID	r²[population]
rs1383846	0.82[ASN][1000 genomes]
rs1383847	0.95[ASN][1000 genomes]
rs1481526	0.81[ASN][1000 genomes]
rs1481529	0.81[ASN][1000 genomes]
rs1481551	0.82[ASN][1000 genomes]
rs1531731	0.82[ASN][1000 genomes]
rs1531732	0.96[ASN][1000 genomes]
rs1600780	0.81[ASN][1000 genomes]
rs2128025	0.85[ASN][1000 genomes]
rs2448966	0.81[ASN][1000 genomes]
rs2464140	0.82[ASN][1000 genomes]
rs2470692	0.82[ASN][1000 genomes]
rs2623318	0.81[ASN][1000 genomes]
rs2623374	0.82[ASN][1000 genomes]
rs2623376	0.81[ASN][1000 genomes]
rs2700586	0.83[ASN][1000 genomes]
rs2700587	0.92[ASN][1000 genomes]
rs2700599	0.81[ASN][1000 genomes]
rs2700626	0.96[ASN][1000 genomes]
rs2700627	0.82[ASN][1000 genomes]
rs2700635	0.81[ASN][1000 genomes]
rs2700647	0.83[ASN][1000 genomes]
rs2700648	0.83[ASN][1000 genomes]
rs2700667	0.84[ASN][1000 genomes]
rs2700668	0.82[ASN][1000 genomes]
rs2929443	0.96[ASN][1000 genomes]
rs2951493	0.81[ASN][1000 genomes]
rs900057	0.82[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	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv530026	chr3:98837320-99340537	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv877216	chr3:99065296-99161022	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99070000-99070400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr3:99070000-99070400	Enhancers	Adipose Nuclei	Adipose
3	chr3:99070000-99071000	Enhancers	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links