Variant report

Variant	rs6586447
Chromosome Location	chr1:104785902-104785903
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10158447	0.85[ASN][1000 genomes]
rs11185403	0.85[ASN][1000 genomes]
rs11185404	0.84[ASN][1000 genomes]
rs11185405	0.85[ASN][1000 genomes]
rs11185406	0.85[ASN][1000 genomes]
rs12026506	0.83[ASN][1000 genomes]
rs12121548	0.85[ASN][1000 genomes]
rs12126550	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12129522	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12129901	0.85[ASN][1000 genomes]
rs12130258	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12406466	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1497679	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1497680	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1887907	0.85[ASN][1000 genomes]
rs1928305	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1928306	0.85[ASN][1000 genomes]
rs1928317	0.85[ASN][1000 genomes]
rs1928318	0.85[ASN][1000 genomes]
rs1928319	0.85[ASN][1000 genomes]
rs1928320	0.85[ASN][1000 genomes]
rs1928322	0.84[ASN][1000 genomes]
rs1928323	0.85[ASN][1000 genomes]
rs1928324	0.85[ASN][1000 genomes]
rs1928325	0.85[ASN][1000 genomes]
rs1928326	0.85[ASN][1000 genomes]
rs1928327	0.85[ASN][1000 genomes]
rs2209954	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2225250	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2317080	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35094251	0.83[ASN][1000 genomes]
rs3866247	0.85[ASN][1000 genomes]
rs3897240	0.85[ASN][1000 genomes]
rs4571975	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5001661	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6659163	0.83[ASN][1000 genomes]
rs6667359	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6675138	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6675141	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6683449	0.85[ASN][1000 genomes]
rs6683559	0.85[ASN][1000 genomes]
rs6690531	0.85[ASN][1000 genomes]
rs6692944	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6698522	0.85[ASN][1000 genomes]
rs6700312	0.83[ASN][1000 genomes]
rs6701333	0.80[ASN][1000 genomes]
rs6703626	0.85[ASN][1000 genomes]
rs7412375	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7538302	0.80[ASN][1000 genomes]
rs7547425	0.85[ASN][1000 genomes]
rs7548005	0.85[ASN][1000 genomes]
rs7550688	0.85[ASN][1000 genomes]
rs949926	0.83[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	nsv872072	chr1:104470622-105076810	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1010903	chr1:104483363-105468941	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr1:104775600-104790200	Weak transcription	Fetal Heart	heart
2	chr1:104785200-104787400	Weak transcription	Fetal Lung	lung

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