Variant report

Variant	rs971084
Chromosome Location	chr3:140899404-140899405
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10470445	0.81[ASN][1000 genomes]
rs1115183	0.95[ASN][1000 genomes]
rs1154785	0.86[EUR][1000 genomes]
rs11708182	0.90[EUR][1000 genomes]
rs12494551	0.88[EUR][1000 genomes]
rs13068771	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1397798	0.86[JPT][hapmap]
rs1511370	0.86[JPT][hapmap]
rs1511381	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1511383	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1511385	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1511386	0.85[JPT][hapmap]
rs1533129	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1912730	0.95[ASN][1000 genomes]
rs1949114	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2169867	0.95[ASN][1000 genomes]
rs2169868	1.00[JPT][hapmap]
rs2311499	0.97[ASN][1000 genomes]
rs4308250	0.88[JPT][hapmap]
rs4683568	0.95[ASN][1000 genomes]
rs4683571	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4683573	0.84[ASN][1000 genomes]
rs6439984	1.00[JPT][hapmap]
rs6439985	0.86[JPT][hapmap]
rs6776346	0.84[ASN][1000 genomes]
rs6800524	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6809691	0.95[ASN][1000 genomes]
rs7613134	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7632734	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7635370	0.88[EUR][1000 genomes]
rs899344	0.88[EUR][1000 genomes]
rs9289620	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9289622	0.87[ASN][1000 genomes]
rs971085	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs985627	0.95[ASN][1000 genomes]
rs9859339	0.87[ASN][1000 genomes]
rs995782	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs995784	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9990218	0.85[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877550	chr3:140867094-140933231	Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	4 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	chr3:140898200-140906000	Weak transcription	Fetal Muscle Trunk	muscle

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