Variant report

Variant	rs9348655
Chromosome Location	chr6:25023263-25023264
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs441342	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6906443	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6907293	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6929342	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6929348	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6929749	0.84[AMR][1000 genomes]
rs6934141	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9295644	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9348656	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9348657	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9348658	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9348659	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9356953	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9356954	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9356955	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9356956	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9356957	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9356958	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9358821	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9358822	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9358823	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9358824	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9358825	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9358826	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9366595	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9366596	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9366597	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9366598	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9366599	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9379706	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9379707	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9393607	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9393608	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9461090	0.86[ASN][1000 genomes]
rs9467378	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[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	nsv1022966	chr6:24763776-25154212	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv538160	chr6:24763776-25154212	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv883482	chr6:24926730-25035920	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1023989	chr6:24930362-25285679	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv1030634	chr6:24938277-25040161	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv830610	chr6:24951741-25124239	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
7	nsv981111	chr6:25023198-25024891	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25011200-25023400	Weak transcription	Thymus	Thymus
2	chr6:25011200-25035600	Weak transcription	Spleen	Spleen
3	chr6:25015600-25023600	Weak transcription	Fetal Thymus	thymus
4	chr6:25015800-25023800	Weak transcription	Dnd41	blood
5	chr6:25015800-25027000	Weak transcription	Esophagus	oesophagus
6	chr6:25017000-25023800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:25018200-25023400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr6:25018200-25023600	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr6:25018200-25023600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr6:25018200-25025000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:25018200-25027400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr6:25018400-25023600	Weak transcription	Primary hematopoietic stem cells	blood
13	chr6:25018400-25023600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr6:25018400-25024600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr6:25018400-25025000	Weak transcription	Primary T cells from cord blood	blood
16	chr6:25018400-25025000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr6:25018400-25025600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr6:25018600-25023600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr6:25018600-25024000	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr6:25018600-25024800	Weak transcription	HMEC	breast
21	chr6:25018600-25025000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr6:25018600-25026000	Weak transcription	Primary B cells from peripheral blood	blood
23	chr6:25019200-25023400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:25022800-25024800	Weak transcription	NHEK	skin
25	chr6:25022800-25025200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr6:25023000-25024600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr6:25023000-25024600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:25023200-25024600	Strong transcription	Primary T cells fromperipheralblood	blood

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