Variant report

Variant	rs2831125
Chromosome Location	chr21:29073983-29073984
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:28222055..28222830-chr21:29073096..29074079,2	K562	blood:
2	chr21:28221585..28222726-chr21:29073735..29074729,3	MCF-7	breast:
3	chr21:28221411..28222029-chr21:29073057..29074050,3	K562	blood:
4	chr21:28221528..28223154-chr21:29072525..29074611,26	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs2831104	0.81[AMR][1000 genomes]
rs2831105	0.87[EUR][1000 genomes]
rs2831106	0.87[EUR][1000 genomes]
rs2831108	0.94[EUR][1000 genomes]
rs2831109	0.94[EUR][1000 genomes]
rs2831111	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831112	0.81[AMR][1000 genomes]
rs2831113	0.81[AMR][1000 genomes]
rs2831114	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831115	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831116	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831117	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831118	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831119	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831120	0.81[AMR][1000 genomes]
rs2831121	0.81[AMR][1000 genomes]
rs2831122	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831123	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831124	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2831127	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28372648	0.94[EUR][1000 genomes]
rs28447510	0.81[AMR][1000 genomes]
rs28464665	0.81[AMR][1000 genomes]
rs28481440	0.94[EUR][1000 genomes]
rs57834801	0.87[EUR][1000 genomes]
rs57891571	1.00[EUR][1000 genomes]
rs7275805	0.81[AMR][1000 genomes]
rs7277044	0.81[AMR][1000 genomes]
rs7282926	0.81[AMR][1000 genomes]
rs73386097	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8133174	0.93[EUR][1000 genomes]
rs9305330	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9980330	0.87[EUR][1000 genomes]
rs9982894	0.81[AMR][1000 genomes]
rs9982905	0.81[AMR][1000 genomes]
rs9983150	0.81[AMR][1000 genomes]
rs9983153	0.81[AMR][1000 genomes]
rs9983357	0.81[AMR][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:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:29067400-29076000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr21:29073000-29074400	Enhancers	Fetal Lung	lung
3	chr21:29073200-29075800	Weak transcription	NHDF-Ad	bronchial
4	chr21:29073400-29074000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr21:29073600-29074000	Enhancers	Fetal Kidney	kidney
6	chr21:29073600-29074000	Flanking Active TSS	Osteobl	bone
7	chr21:29073800-29074000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
8	chr21:29073800-29075600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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