Variant report

Variant	rs61870569
Chromosome Location	chr10:116551722-116551723
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11593472	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11598354	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12761207	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12761991	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12763449	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12763784	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12767625	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12767713	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12783562	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12785140	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17720374	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17794002	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34105246	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34202625	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34366626	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34751270	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35736355	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35927479	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs36021781	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs55633935	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58719367	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59254826	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7073405	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7075095	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7080890	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7082250	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7092145	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7902647	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7919367	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7922771	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs808325	0.84[AMR][1000 genomes];0.84[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	nsv949138	chr10:116311531-116874477	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1038050	chr10:116315109-116895719	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv533027	chr10:116344641-116856352	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	esv3435429	chr10:116394152-117006347	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	esv1814163	chr10:116519705-116582581	Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv516803	chr10:116528294-116556846	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116540600-116553000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr10:116540800-116553200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr10:116549000-116556000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr10:116549200-116554800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:116549400-116553200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr10:116549400-116553400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr10:116550600-116552000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr10:116550800-116552200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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