Variant report

Variant	rs16971562
Chromosome Location	chr15:41459786-41459787
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:41456615..41459900-chr15:41462571..41464669,4	K562	blood:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs12324568	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13329240	0.91[ASN][1000 genomes]
rs16952331	0.82[CEU][hapmap];0.92[CHB][hapmap];0.81[JPT][hapmap];0.89[EUR][1000 genomes]
rs16971576	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16971647	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16971651	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16971653	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16971654	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16971734	0.81[EUR][1000 genomes]
rs2083238	0.94[EUR][1000 genomes]
rs2090826	1.00[CEU][hapmap];0.93[CHB][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2118739	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2305656	0.88[JPT][hapmap]
rs2412607	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2412610	0.82[CEU][hapmap];0.84[CHB][hapmap];0.86[EUR][1000 genomes]
rs28889391	0.81[ASN][1000 genomes]
rs2899014	0.86[EUR][1000 genomes]
rs55787465	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55952963	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56262456	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56815966	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57009745	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57896923	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58060180	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58322837	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58436082	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58851405	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59441380	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59500750	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs60789744	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6492995	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs7165551	1.00[CEU][hapmap];0.93[CHB][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7166182	1.00[CEU][hapmap];0.93[CHB][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7167142	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7168706	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7172299	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7173545	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73394302	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs74012251	0.92[EUR][1000 genomes]
rs74012252	0.92[EUR][1000 genomes]
rs74012253	0.88[EUR][1000 genomes]
rs74012255	0.81[EUR][1000 genomes]
rs8025660	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8025916	1.00[CEU][hapmap];0.92[CHB][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8026570	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8029385	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8029694	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8030683	1.00[CEU][hapmap];0.92[CHB][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8030706	1.00[CEU][hapmap];0.93[CHB][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8030712	1.00[CEU][hapmap];0.92[CHB][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8030732	1.00[CEU][hapmap];0.92[CHB][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8030954	1.00[CEU][hapmap];0.92[CHB][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8031542	1.00[CEU][hapmap];0.84[CHB][hapmap];0.90[EUR][1000 genomes]
rs8038103	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8038575	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8039060	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8040375	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9672272	0.88[EUR][1000 genomes]
rs9672309	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9745300	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9796	0.88[JPT][hapmap]

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	nsv569229	chr15:41361138-41483682	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv904107	chr15:41361138-41493013	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv569230	chr15:41384649-41483682	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv904108	chr15:41384649-41486990	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
5	nsv904109	chr15:41410705-41481254	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv457120	chr15:41410705-41546631	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv569231	chr15:41410705-41546631	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41458800-41461200	Weak transcription	Primary hematopoietic stem cells	blood

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