Variant report

Variant	rs35746743
Chromosome Location	chr7:67318331-67318332
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12666343	0.84[ASN][1000 genomes]
rs12670521	1.00[AFR][1000 genomes]
rs12698625	0.95[ASN][1000 genomes]
rs13238059	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13242525	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13244158	0.86[ASN][1000 genomes]
rs2864463	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2902759	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2902836	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34752925	0.81[ASN][1000 genomes]
rs35227483	0.88[ASN][1000 genomes]
rs35712623	0.86[ASN][1000 genomes]
rs35850158	0.91[ASN][1000 genomes]
rs3846975	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4718638	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4718641	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62458311	0.95[ASN][1000 genomes]
rs62458316	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6946477	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6951285	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6955469	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6955571	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6973904	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6975069	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71535653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71535654	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[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	nsv1027532	chr7:67261526-67387398	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:67317600-67319800	Enhancers	Fetal Brain Male	brain
2	chr7:67317800-67319000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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