Variant report

Variant	rs61848626
Chromosome Location	chr10:50577305-50577306
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:50575926..50578521-chr10:50603618..50605883,2	K562	blood:
2	chr10:50562650..50564332-chr10:50576069..50577955,2	K562	blood:
3	chr10:50576804..50578658-chr10:50581839..50584032,2	K562	blood:
4	chr10:50571360..50573134-chr10:50577043..50579272,2	K562	blood:
5	chr10:50185577..50187272-chr10:50575569..50577378,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128815	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10508913	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12572851	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12572858	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17009950	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17009953	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17009956	0.80[AFR][1000 genomes]
rs17009957	0.80[AFR][1000 genomes]
rs17009961	0.81[AFR][1000 genomes]
rs17176872	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17176977	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17177005	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17783577	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17783607	0.87[EUR][1000 genomes]
rs3849153	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4012237	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41301105	0.86[EUR][1000 genomes]
rs57455400	0.92[EUR][1000 genomes]
rs58733378	0.81[AFR][1000 genomes]
rs61848624	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848625	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61848627	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848634	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848635	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848637	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848639	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848642	0.88[EUR][1000 genomes]
rs61848644	0.88[EUR][1000 genomes]
rs61848646	0.86[EUR][1000 genomes]
rs61850964	0.84[EUR][1000 genomes]
rs73311930	0.83[EUR][1000 genomes]
rs7915692	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7916121	0.94[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	nsv526843	chr10:50570544-50585177	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50576800-50577400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:50577000-50577600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:50577000-50578200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr10:50577200-50578200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:50577200-50578200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr10:50577200-50578200	Enhancers	HUVEC	blood vessel

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