Variant report

Variant	rs62158282
Chromosome Location	chr2:67537344-67537345
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:67521312..67523187-chr2:67535421..67537676,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs12988210	0.83[AFR][1000 genomes]
rs12996359	0.83[AFR][1000 genomes]
rs13015319	0.83[AFR][1000 genomes]
rs13016330	0.83[AFR][1000 genomes]
rs13018272	0.83[AFR][1000 genomes]
rs13026513	0.83[AFR][1000 genomes]
rs1384743	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs1384744	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs17544516	0.83[AFR][1000 genomes]
rs17544551	0.83[AFR][1000 genomes]
rs17603029	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs17603914	0.83[AFR][1000 genomes]
rs2170703	0.88[EUR][1000 genomes]
rs2171176	0.83[AFR][1000 genomes]
rs34262449	0.83[AFR][1000 genomes]
rs34274370	0.83[AFR][1000 genomes]
rs34281542	0.83[AFR][1000 genomes]
rs34286589	0.83[AFR][1000 genomes]
rs34547630	0.83[AFR][1000 genomes]
rs34636997	0.83[AFR][1000 genomes]
rs34997300	0.83[AFR][1000 genomes]
rs35141978	0.83[AFR][1000 genomes]
rs35570926	0.83[AFR][1000 genomes]
rs35607813	0.83[AFR][1000 genomes]
rs35610403	0.83[AFR][1000 genomes]
rs4274583	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4605358	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56880806	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs58349979	0.88[EUR][1000 genomes]
rs60181254	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62146349	0.83[AFR][1000 genomes]
rs62154898	0.83[AFR][1000 genomes]
rs62154949	0.83[AFR][1000 genomes]
rs62154950	0.83[AFR][1000 genomes]
rs62154951	0.83[AFR][1000 genomes]
rs62154952	0.83[AFR][1000 genomes]
rs62156538	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs62156540	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs62156541	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs62156542	0.85[EUR][1000 genomes]
rs62156547	0.88[EUR][1000 genomes]
rs62158280	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62158281	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62158290	0.83[AFR][1000 genomes]
rs6741192	0.87[EUR][1000 genomes]
rs7573357	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7606736	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs874236	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv834249	chr2:67515471-67691605	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67532000-67538800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:67535400-67539400	Enhancers	NHDF-Ad	bronchial
3	chr2:67535800-67538400	Enhancers	Fetal Lung	lung
4	chr2:67536000-67537400	Enhancers	HepG2	liver
5	chr2:67536200-67537400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr2:67536400-67539200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:67536400-67539400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr2:67536600-67538200	Weak transcription	NHLF	lung
9	chr2:67536800-67538200	Weak transcription	NH-A	brain
10	chr2:67536800-67538600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr2:67536800-67538600	Weak transcription	Hela-S3	cervix
12	chr2:67537000-67538600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr2:67537000-67538800	Weak transcription	A549	lung
14	chr2:67537200-67538800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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