Variant report

Variant	rs35894621
Chromosome Location	chr3:98741032-98741033
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10589669	0.91[AMR][1000 genomes]
rs12107272	0.82[EUR][1000 genomes]
rs13065136	0.82[EUR][1000 genomes]
rs13074614	0.91[AMR][1000 genomes]
rs13074787	0.91[AMR][1000 genomes]
rs13076960	0.91[AMR][1000 genomes]
rs13079960	0.86[EUR][1000 genomes]
rs13081992	0.82[EUR][1000 genomes]
rs13083238	0.91[AMR][1000 genomes]
rs13083934	0.91[AMR][1000 genomes]
rs13084692	0.91[AMR][1000 genomes]
rs13087627	0.83[AMR][1000 genomes]
rs13087631	0.91[AMR][1000 genomes]
rs13096085	0.82[EUR][1000 genomes]
rs13097876	0.82[EUR][1000 genomes]
rs13100915	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13100937	0.82[EUR][1000 genomes]
rs34008360	0.91[AMR][1000 genomes]
rs34269725	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34279227	0.91[AMR][1000 genomes]
rs34284740	0.82[EUR][1000 genomes]
rs34394867	0.86[EUR][1000 genomes]
rs34428696	0.83[AMR][1000 genomes]
rs34458031	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34479374	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs34489202	0.83[AMR][1000 genomes]
rs34711372	0.91[AMR][1000 genomes]
rs34725039	0.82[EUR][1000 genomes]
rs34791359	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34826460	0.82[EUR][1000 genomes]
rs34848749	0.91[AMR][1000 genomes]
rs34860591	0.91[AMR][1000 genomes]
rs35025156	0.82[EUR][1000 genomes]
rs35098355	0.91[AMR][1000 genomes]
rs35103318	0.82[EUR][1000 genomes]
rs35219252	0.91[AMR][1000 genomes]
rs35234681	0.84[EUR][1000 genomes]
rs35239055	0.91[AMR][1000 genomes]
rs35312318	0.82[EUR][1000 genomes]
rs35366262	0.91[AMR][1000 genomes]
rs35422064	0.91[AMR][1000 genomes]
rs35499232	0.82[EUR][1000 genomes]
rs35514544	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35539438	0.91[AMR][1000 genomes]
rs35592768	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs35764973	0.82[EUR][1000 genomes]
rs35914268	0.91[AMR][1000 genomes]
rs35947493	0.86[EUR][1000 genomes]
rs35947806	0.91[AMR][1000 genomes]
rs36028944	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs36098932	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs36157152	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56083233	0.82[EUR][1000 genomes]
rs56246599	0.82[EUR][1000 genomes]
rs56408882	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs6764579	0.84[EUR][1000 genomes]
rs6805362	0.91[AMR][1000 genomes]
rs71311398	0.91[AMR][1000 genomes]
rs71311402	0.91[AMR][1000 genomes]
rs71313508	0.82[EUR][1000 genomes]
rs71313509	0.82[EUR][1000 genomes]
rs71313510	0.82[EUR][1000 genomes]
rs71313511	0.82[EUR][1000 genomes]
rs71313512	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv591065	chr3:98204198-98766326	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv980100	chr3:98714787-98766962	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv963577	chr3:98736986-98766962	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 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	chr3:98740400-98741200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:98740400-98741200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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