Variant report

Variant	rs2822772
Chromosome Location	chr21:15939544-15939545
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:15937940..15940141-chr21:15954473..15956452,2	K562	blood:
2	chr21:15930237..15934475-chr21:15937814..15942130,5	K562	blood:
3	chr21:15914500..15916247-chr21:15937941..15940190,2	K562	blood:
4	chr21:15938738..15940240-chr21:15946079..15949018,2	K562	blood:

Variant related genes	Relation type
ENSG00000223662	Chromatin interaction
ENSG00000155307	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1022446	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1556281	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs2178936	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2178937	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2178938	1.00[ASN][1000 genomes]
rs2223091	0.85[CHB][hapmap]
rs2249923	0.82[AFR][1000 genomes]
rs2822769	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2822773	0.82[AFR][1000 genomes]
rs28429627	0.97[ASN][1000 genomes]
rs28701010	0.97[ASN][1000 genomes]
rs4817236	0.89[JPT][hapmap]
rs6516877	0.84[CHB][hapmap];0.84[JPT][hapmap]
rs6516888	0.92[YRI][hapmap];0.86[AFR][1000 genomes]
rs66740377	0.80[ASN][1000 genomes]
rs7278952	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7281104	0.84[CHB][hapmap];0.84[JPT][hapmap]
rs8128727	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs989938	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9978243	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9980028	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs9980764	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs9982259	0.82[CHB][hapmap]
rs9982591	1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs9983058	0.88[AFR][1000 genomes]
rs9983068	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9983327	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1059591	chr21:15835325-15969195	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1056423	chr21:15838309-15948474	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv544376	chr21:15855470-15948474	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1065823	chr21:15863224-15948474	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1057934	chr21:15863224-15969195	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1058533	chr21:15896056-15948474	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv544377	chr21:15896056-15948474	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv834045	chr21:15900678-16112850	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv834046	chr21:15903792-16077369	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15938200-15940200	Enhancers	K562	blood
2	chr21:15938400-15939800	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr21:15938800-15943400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr21:15939000-15939800	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr21:15939200-15940200	Enhancers	Fetal Thymus	thymus
6	chr21:15939400-15940400	Weak transcription	Primary B cells from cord blood	blood
7	chr21:15939400-15940400	Enhancers	Dnd41	blood
8	chr21:15939400-15940600	Flanking Active TSS	GM12878-XiMat	blood
9	chr21:15939400-15942000	Enhancers	Primary B cells from peripheral blood	blood

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