Variant report

Variant	rs61848637
Chromosome Location	chr10:50587957-50587958
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:50587898..50588680-chr10:50601547..50602465,2	K562	blood:
2	chr10:50586997..50589481-chr10:50594678..50597355,2	MCF-7	breast:
3	chr10:50185069..50185664-chr10:50587382..50588272,2	MCF-7	breast:
4	chr10:50372128..50374290-chr10:50587690..50589612,2	K562	blood:
5	chr10:50586751..50588535-chr10:50592875..50594990,2	K562	blood:
6	chr10:50578807..50581361-chr10:50585361..50588030,3	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10508913	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12572851	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12572858	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17009950	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17009953	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17176872	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17176977	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17177005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17783577	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17783607	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3849153	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4012237	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41301105	0.96[EUR][1000 genomes]
rs57455400	0.97[EUR][1000 genomes]
rs61848624	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848625	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61848626	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848627	0.86[AFR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848634	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848635	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61848642	0.83[EUR][1000 genomes]
rs61848644	0.83[EUR][1000 genomes]
rs61848646	0.96[EUR][1000 genomes]
rs61850964	0.93[EUR][1000 genomes]
rs73311930	0.87[EUR][1000 genomes]
rs7915692	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7916121	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50587800-50588200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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