Variant report

Variant	rs981539
Chromosome Location	chr10:44931333-44931334
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:44931249..44933954-chr10:44941041..44943076,2	MCF-7	breast:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11239040	1.00[EUR][1000 genomes]
rs1147942	1.00[EUR][1000 genomes]
rs1147945	1.00[EUR][1000 genomes]
rs1147946	1.00[EUR][1000 genomes]
rs1147947	1.00[EUR][1000 genomes]
rs1147951	1.00[EUR][1000 genomes]
rs1147953	1.00[EUR][1000 genomes]
rs1147955	1.00[EUR][1000 genomes]
rs1147959	1.00[EUR][1000 genomes]
rs1147964	1.00[EUR][1000 genomes]
rs12244007	1.00[EUR][1000 genomes]
rs1253715	1.00[EUR][1000 genomes]
rs1253717	1.00[EUR][1000 genomes]
rs1334314	1.00[EUR][1000 genomes]
rs1413515	0.93[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1413516	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1572206	1.00[EUR][1000 genomes]
rs17156124	1.00[EUR][1000 genomes]
rs1889922	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs197454	1.00[EUR][1000 genomes]
rs491494	1.00[EUR][1000 genomes]
rs56908169	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58512899	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58837754	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60579789	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61215910	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs639840	1.00[EUR][1000 genomes]
rs6593414	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7069446	1.00[EUR][1000 genomes]
rs7069784	1.00[EUR][1000 genomes]
rs7075428	1.00[EUR][1000 genomes]
rs7075562	1.00[EUR][1000 genomes]
rs7075568	1.00[EUR][1000 genomes]
rs7083225	1.00[EUR][1000 genomes]
rs7090818	0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7094628	1.00[EUR][1000 genomes]
rs7095527	1.00[EUR][1000 genomes]
rs7895274	1.00[EUR][1000 genomes]
rs7898252	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7909675	1.00[EUR][1000 genomes]
rs883915	1.00[EUR][1000 genomes]
rs928566	1.00[EUR][1000 genomes]
rs9663451	1.00[EUR][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	nsv895101	chr10:44909081-45007131	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv550701	chr10:44913113-44935055	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 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	chr10:44930600-44931600	Weak transcription	Adipose Nuclei	Adipose

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