Variant report

Variant	rs7916121
Chromosome Location	chr10:50589372-50589373
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:50586997..50589481-chr10:50594678..50597355,2	MCF-7	breast:
2	chr10:50372128..50374290-chr10:50587690..50589612,2	K562	blood:
3	chr10:50541425..50543053-chr10:50588433..50591403,2	MCF-7	breast:
4	chr10:50589316..50590909-chr10:50591054..50594050,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10508913	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12572851	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12572858	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1570645	0.82[AFR][1000 genomes]
rs17009950	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17009953	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17176872	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17176977	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17177005	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17783577	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17783607	0.89[EUR][1000 genomes]
rs1977293	0.83[AFR][1000 genomes]
rs3849153	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4012237	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41301105	0.88[EUR][1000 genomes]
rs57455400	0.86[EUR][1000 genomes]
rs61848624	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848625	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61848626	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848627	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848634	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848635	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848637	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848639	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848642	0.89[EUR][1000 genomes]
rs61848644	0.89[EUR][1000 genomes]
rs61848646	0.88[EUR][1000 genomes]
rs61850964	0.85[EUR][1000 genomes]
rs73311930	0.84[EUR][1000 genomes]
rs7915692	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv895377	chr10:50588990-50678212	ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50588000-50591000	Weak transcription	Right Atrium	heart
2	chr10:50588200-50591600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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