Variant report

Variant	rs10484982
Chromosome Location	chr6:54460482-54460483
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10484983	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484986	0.84[AMR][1000 genomes]
rs10484991	0.82[CEU][hapmap]
rs10948828	0.84[EUR][1000 genomes]
rs12333325	0.84[AMR][1000 genomes]
rs1395625	0.82[CEU][hapmap]
rs16885517	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16885549	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16885553	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16885557	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16885559	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16885565	0.84[AMR][1000 genomes]
rs16885575	0.84[AMR][1000 genomes]
rs16885845	0.82[CEU][hapmap]
rs16885849	0.82[CEU][hapmap]
rs17448241	1.00[CEU][hapmap]
rs17545325	1.00[CEU][hapmap]
rs60428561	0.84[EUR][1000 genomes]
rs6459015	0.84[EUR][1000 genomes]
rs6909601	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6918025	0.84[EUR][1000 genomes]
rs73742133	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9296762	0.82[CEU][hapmap]
rs9464100	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9464102	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9474926	0.84[AMR][1000 genomes]
rs9474927	0.84[AMR][1000 genomes]
rs9474928	0.84[AMR][1000 genomes]
rs9474929	0.84[AMR][1000 genomes]
rs9474930	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427757	chr6:54296552-54507210	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv885890	chr6:54339930-54460646	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv885893	chr6:54344853-54460646	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv885897	chr6:54350048-54460646	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54460200-54461600	Enhancers	Osteobl	bone
2	chr6:54460400-54461400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:54460400-54461400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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