Variant report

Variant	rs62167168
Chromosome Location	chr2:151867554-151867555
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:151867304..151868964-chr2:151869029..151870769,2	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12612667	1.00[AFR][1000 genomes]
rs12613613	1.00[AFR][1000 genomes]
rs12617947	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs12619845	1.00[AFR][1000 genomes]
rs12620371	1.00[AFR][1000 genomes]
rs12623677	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs16828997	1.00[AFR][1000 genomes]
rs16829081	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs16829215	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs16829234	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs41478047	1.00[AFR][1000 genomes]
rs62167120	1.00[AFR][1000 genomes]
rs62167121	1.00[AFR][1000 genomes]
rs62167165	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62167166	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs62167167	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs62167191	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs62168566	1.00[AFR][1000 genomes]
rs62168569	1.00[AFR][1000 genomes]
rs62168572	1.00[AFR][1000 genomes]
rs62168573	1.00[AFR][1000 genomes]
rs62168579	1.00[AFR][1000 genomes]
rs62168581	1.00[AFR][1000 genomes]
rs62168583	1.00[AFR][1000 genomes]
rs62168596	1.00[AFR][1000 genomes]
rs62168623	1.00[AFR][1000 genomes]
rs62168625	1.00[AFR][1000 genomes]
rs62168631	1.00[AFR][1000 genomes]
rs62168641	1.00[AFR][1000 genomes]
rs62168642	1.00[AFR][1000 genomes]
rs62169389	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs62169390	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs62169391	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs62169392	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs62169395	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs62169396	1.00[AFR][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	nsv525350	chr2:151711700-152044794	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv523849	chr2:151718133-152143524	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	esv3693426	chr2:151725792-152295862	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1002140	chr2:151833257-152054910	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv438373	chr2:151864071-151869808	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151843800-151871000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:151865600-151872800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:151867200-151867800	Enhancers	Fetal Brain Female	brain

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