Variant report

Variant	rs12537432
Chromosome Location	chr7:71397521-71397522
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:71389179..71391286-chr7:71396356..71398267,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10227914	0.90[CHB][hapmap]
rs10447536	1.00[JPT][hapmap]
rs10950287	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11763822	0.82[JPT][hapmap]
rs11766067	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11766746	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769248	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs12537492	0.90[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16869589	0.89[CHB][hapmap]
rs17340451	1.00[JPT][hapmap]
rs17340639	1.00[JPT][hapmap]
rs17424992	1.00[JPT][hapmap]
rs17425888	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs2023988	0.82[JPT][hapmap]
rs2158656	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs2867559	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs35956175	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61072003	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs66473905	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66945198	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67149594	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67522636	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67676824	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6944606	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs6946044	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6961327	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6965098	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs6968074	0.82[JPT][hapmap]
rs726469	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs73185091	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs733909	0.82[JPT][hapmap]
rs7349979	0.82[JPT][hapmap]
rs769022	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7776793	0.88[CHB][hapmap];0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026896	chr7:71003462-71721516	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1027496	chr7:71162362-71575116	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916220	chr7:71200006-71708048	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv531372	chr7:71300090-71909517	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	nsv1017367	chr7:71339782-71476575	ZNF genes & repeats Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71393200-71400000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr7:71393400-71398400	Weak transcription	Fetal Thymus	thymus
3	chr7:71396400-71398200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:71397000-71399600	Weak transcription	Thymus	Thymus
5	chr7:71397200-71398800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:71397200-71400000	Weak transcription	Primary hematopoietic stem cells	blood

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