Variant report

Variant	rs12482497
Chromosome Location	chr21:29064065-29064066
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11702066	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12482624	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12483350	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12483741	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs16980990	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16981008	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16981014	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2831041	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2831042	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2831043	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2831044	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2831045	0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2831048	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2831049	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2831050	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2831053	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4817183	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57688665	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7275935	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7278716	0.82[ASN][1000 genomes]
rs73384066	0.85[ASN][1000 genomes]
rs73384078	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs73384086	0.92[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73386055	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73386080	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs928273	0.89[AMR][1000 genomes];0.84[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	nsv459229	chr21:28543456-29482488	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv587342	chr21:28543456-29482488	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1059423	chr21:28957144-29306656	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv913670	chr21:29022265-29525767	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv1059134	chr21:29061408-29188185	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:29062600-29064800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr21:29063400-29065400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr21:29063800-29064800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr21:29063800-29065400	Weak transcription	HSMM	muscle
5	chr21:29064000-29065000	Weak transcription	Osteobl	bone
6	chr21:29064000-29066400	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links