Variant report

Variant	rs6583682
Chromosome Location	chr10:91842555-91842556
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10159518	0.84[EUR][1000 genomes]
rs10160072	0.84[EUR][1000 genomes]
rs10160077	0.84[EUR][1000 genomes]
rs10160169	0.84[EUR][1000 genomes]
rs10736055	0.81[EUR][1000 genomes]
rs10748537	0.84[EUR][1000 genomes]
rs10785938	0.81[EUR][1000 genomes]
rs10785939	0.81[EUR][1000 genomes]
rs12264971	0.81[EUR][1000 genomes]
rs1325734	0.81[EUR][1000 genomes]
rs1329164	0.84[EUR][1000 genomes]
rs1329165	0.84[EUR][1000 genomes]
rs1329166	0.84[EUR][1000 genomes]
rs1359549	0.81[EUR][1000 genomes]
rs1410899	0.84[EUR][1000 genomes]
rs1575795	0.84[EUR][1000 genomes]
rs1590823	0.84[EUR][1000 genomes]
rs1813172	0.85[EUR][1000 genomes]
rs1854459	0.81[EUR][1000 genomes]
rs2094121	0.81[EUR][1000 genomes]
rs2148024	0.84[EUR][1000 genomes]
rs2419364	0.84[EUR][1000 genomes]
rs2419365	0.84[EUR][1000 genomes]
rs2419366	0.84[EUR][1000 genomes]
rs4933173	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4933534	0.81[EUR][1000 genomes]
rs4933535	0.83[EUR][1000 genomes]
rs4933539	0.83[EUR][1000 genomes]
rs4933541	0.84[EUR][1000 genomes]
rs4933545	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4933546	0.81[EUR][1000 genomes]
rs4933547	0.85[EUR][1000 genomes]
rs6583681	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6583685	0.84[EUR][1000 genomes]
rs7070170	0.81[EUR][1000 genomes]
rs7071916	0.81[EUR][1000 genomes]
rs7072040	0.81[EUR][1000 genomes]
rs7084327	0.80[EUR][1000 genomes]
rs7084467	0.84[EUR][1000 genomes]
rs7085546	0.84[EUR][1000 genomes]
rs7095153	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7097675	0.83[EUR][1000 genomes]
rs7394365	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7394397	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7897322	0.81[EUR][1000 genomes]
rs9971108	0.83[EUR][1000 genomes]
rs9971206	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043571	chr10:91568555-92036154	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv551874	chr10:91570211-92036154	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv949678	chr10:91589048-92016474	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv895883	chr10:91610601-92195828	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1039731	chr10:91645718-92198264	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv540743	chr10:91645718-92198264	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv467430	chr10:91681344-92297943	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv551875	chr10:91681344-92297943	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	esv1839881	chr10:91762226-91861413	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv519094	chr10:91769945-91927196	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91820000-91860000	Weak transcription	Primary B cells from cord blood	blood
2	chr10:91839400-91846600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:91840400-91846600	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr10:91840400-91846600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr10:91840600-91843200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr10:91840600-91846600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr10:91840600-91847000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr10:91840800-91842800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr10:91840800-91846400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr10:91841200-91842800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr10:91842200-91843800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
12	chr10:91842400-91844200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links