Variant report

Variant	rs9796065
Chromosome Location	chr13:94532047-94532048
allele	A/G
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:27)

rs_ID	r²[population]
rs1330459	0.80[EUR][1000 genomes]
rs1411502	0.83[EUR][1000 genomes]
rs1411503	0.80[EUR][1000 genomes]
rs17174714	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2892669	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3858844	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs45608931	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4773764	0.80[EUR][1000 genomes]
rs61962148	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61964364	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61964366	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs713220	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7997761	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9516299	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9516307	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9516309	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9524238	0.81[EUR][1000 genomes]
rs9524244	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9524248	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9524251	0.84[EUR][1000 genomes]
rs9524255	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9524267	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs955129	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9556336	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9561455	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9561456	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9796211	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948714	chr13:94100104-94699435	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv933807	chr13:94187158-94845505	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1045230	chr13:94277683-94764671	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv832684	chr13:94379507-94550853	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv948455	chr13:94451368-94988900	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv430598	chr13:94490519-94546599	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv916640	chr13:94521959-95101443	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:94528000-94533400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr13:94528200-94533800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr13:94531200-94534400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr13:94531400-94534400	Weak transcription	Fetal Stomach	stomach

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