Variant report

Variant	rs2945970
Chromosome Location	chr19:36989005-36989006
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:36978237..36981071-chr19:36988174..36990152,2	K562	blood:
2	chr19:36978237..36981428-chr19:36988174..36990245,3	K562	blood:

Variant related genes	Relation type
ENSG00000186017	Chromatin interaction
ENSG00000267309	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1878927	1.00[CEU][hapmap];0.93[JPT][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2052730	0.90[ASN][1000 genomes]
rs2385796	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2912411	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2912420	1.00[CEU][hapmap];0.85[CHB][hapmap];0.94[JPT][hapmap];0.89[YRI][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2912421	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2912422	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2912424	0.91[ASN][1000 genomes]
rs2912426	0.97[ASN][1000 genomes]
rs2912427	0.87[ASN][1000 genomes]
rs2912428	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2912431	0.99[ASN][1000 genomes]
rs2912434	0.85[ASN][1000 genomes]
rs2912436	0.84[ASN][1000 genomes]
rs2912437	0.90[CHB][hapmap];0.87[JPT][hapmap];0.84[ASN][1000 genomes]
rs2912438	0.86[ASN][1000 genomes]
rs2945946	1.00[CHB][hapmap];0.87[JPT][hapmap];0.92[ASN][1000 genomes]
rs2945954	0.84[AMR][1000 genomes]
rs2945960	0.92[ASN][1000 genomes]
rs2945966	0.87[ASN][1000 genomes]
rs2945967	0.84[ASN][1000 genomes]
rs2945968	0.81[ASN][1000 genomes]
rs2945974	0.90[CHB][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs2945975	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2945977	0.81[ASN][1000 genomes]
rs2945979	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2945980	0.82[ASN][1000 genomes]
rs2945982	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2945987	0.85[ASN][1000 genomes]
rs2945988	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2967432	0.91[ASN][1000 genomes]
rs2967434	0.87[ASN][1000 genomes]
rs2967435	0.85[CHB][hapmap]
rs2967441	0.84[ASN][1000 genomes]
rs2967448	0.90[ASN][1000 genomes]
rs2967449	1.00[CHB][hapmap];0.87[JPT][hapmap];0.89[ASN][1000 genomes]
rs2967450	0.89[CHB][hapmap];0.89[ASN][1000 genomes]
rs2967451	1.00[CHB][hapmap];0.81[JPT][hapmap];0.93[ASN][1000 genomes]
rs2967452	0.80[ASN][1000 genomes]
rs2967456	0.97[ASN][1000 genomes]
rs2967457	0.91[ASN][1000 genomes]
rs2967467	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2967468	0.87[ASN][1000 genomes]
rs2967471	0.89[ASN][1000 genomes]
rs2967474	0.97[ASN][1000 genomes]
rs2967475	0.90[ASN][1000 genomes]
rs2967505	1.00[CHB][hapmap];0.87[JPT][hapmap];0.89[ASN][1000 genomes]
rs2967529	0.84[AMR][1000 genomes]
rs2967532	0.92[CEU][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes]
rs2967533	1.00[CEU][hapmap];0.94[JPT][hapmap];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2967542	0.92[ASN][1000 genomes]
rs2967544	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3107237	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs3107238	0.87[ASN][1000 genomes]
rs3111554	0.93[ASN][1000 genomes]
rs4561584	0.93[ASN][1000 genomes]
rs6510545	0.89[AMR][1000 genomes];0.85[EUR][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	nsv833816	chr19:36824257-37034287	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv1064851	chr19:36910259-37689721	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
3	nsv911648	chr19:36914171-37047472	Weak transcription Active TSS Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	nsv1065698	chr19:36916796-37690124	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
5	nsv543999	chr19:36916796-37690124	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
6	nsv529817	chr19:36930549-37654062	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
7	nsv833817	chr19:36978852-37195695	ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links